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Weekly meetings with medical director (if possible) or weekly communication with medical director, at a minimum. The global medical director can be pulled in if the issue cannot be easily resolved. The Regional Medical Director (RMD) is an integral member of the metabolic/obesity clinical sciences g

pTheWhiteam is seeking a Horizontal Architect to lead and unify tooling, documentation and back-office migrations across Grants and Experts domains. This remote EU role requires strong frontend and backend capabilities, including Angular, Java, REST, and cloud knowledge. /ppYou'll produce technical governance, provide 3rd-level support, and participate in planning and demonstrations, while delivering robust documentation and automation to improve platform reliability. /p #J-18808-Ljbffr

An international client is seeking a Senior BI Developer/Architect to join their remote team. This role involves designing and maintaining business intelligence solutions using AWS QuickSight and Power BI. Candidates should have extensive experience in BI development, strong SQL and data modeling skills, and a solid understanding of AWS data services. Excellent English communication abilities are a must as you will work closely with business stakeholders to translate complex requirements into actionable insights.br#J-18808-Ljbffr

Core Responsibilities- Perform and certify airworthiness maintenance tasks on our fleet, ensuring full compliance with EASA Part‑145 and Volotea’s Maintenance Organization Exposition (MOE).- Work in a blended environment, supporting technical operations remotely and traveling to our operational bases for hands‑on maintenance and certification.- Ensure all maintenance tasks required by the operator are completed or properly deferred, while verifying the impact of any outstanding items on airworthiness and safety.- Review and complete aircraft technical logs and associated documents to ensure accurate and compliant records.- Issue release certificates and technical log entries following maintenance activities, in line with regulatory and company standards.- Support flight crews with technical instructions in the aircraft log when needed.- Contribute to continuous improvement by complying with internal procedures and mandatory reporting.Qualifications- EASA Part 66‑licensed Aircraft Engineer, certified on Airbus A320.- +5 years of hands‑on aircraft maintenance and troubleshooting experience.- Previous experience in Line Maintenance, Maintenance Control, aviation MROs or Airline Engineering.- Strong technical knowledge of aircraft systems and maintenance documentation.- Fluent English (spoken and written); knowledge of Spanish, French, or Italian is a bonus.- Excellent communication, self‑organization, and time‑management skills.- Proactive and cooperative attitude.- Working knowledge of computer systems and programs (especially AMOS, My Boeing Fleet, Airbus World, and AIMS).- Flexible, willing to travel frequently.- Current EASA Regulation (Part M, Part 145), EWIS, and Fuel Tank Safety will be considered a plus.- EU work permit and a valid driver’s license.Benefits- Customize your benefits plan: allocate part of your salary to dining, transport, or health insurance—tax‑free, so you save more.- Well‑being support: discounted gym memberships and coffee to keep you energized.- Enjoy events such as Carnival parties, trips to Port Aventura, ski getaways, running clubs, and paddle & ping‑pong tournaments.Volotea is an equal opportunity employer that values diversity and inclusion and strives to recruit diverse candidates. Our goal is to continuously improve and sustain an inclusive culture by attracting, developing, and engaging the best talent in our industry.

An international technology firm is seeking a Cybersecurity IT Specialist with strong expertise in Splunk to join their multifunctional security operations team. This remote position requires 3 to 5 years of relevant experience, a technical engineering background, and fluency in English. Responsibilities include SIEM monitoring, incident response, and support for security tools. The role offers a competitive rate of €245-255 per day and requires shift rotation and on-call duties.br#J-18808-Ljbffr

Role: System Validation, Platform Qualification Desplácese hacia abajo para obtener una visión general completa de lo que requerirá este trabajo. ¿Es usted el candidato adecuado para esta oportunidad? Location: Spain(100% Remote) Client: Infosys Sal: Market Range Permanent full-time position Requirements and number of open positions 3-5 years- 2 Positions in Open 5-10 Years- 2 Positions in Open 10+ years - 2 Positins in Open Role Overview We are looking for a highly experienced Validation resource with 10+ years of experience in Computerized System Validation (CSV) within the Life Sciences domain. The candidate will lead end-to-end validation activities for enterprise-level software systems and manage teams, stakeholders, and delivery for global programs. Key Responsibilities • Lead end-to-end validation lifecycle (Planning, Risk Assessment, Testing, Release, Periodic Review), • Drive validation strategy for enterprise programs across regions (Europe/Global), • Manage validation teams, allocate work, and ensure timely delivery, • Act as primary point of contact for client stakeholders and leadership, • Lead governance, status reporting, and escalation management, • Author and review validation deliverables (URS, FRS, IQ/OQ/PQ, RTM, Validation Report), • Ensure compliance with 21 CFR Part 11, EU Annex 11, Data Integrity (ALCOA+), • Manage quality processes (Deviation, CAPA, Change Control), • Support regulatory audits and inspection readiness, • Mentor and coach junior resources, build capability within the team, • Drive continuous improvement and standardization of validation processes Managerial Skills • Team leadership and people management, • Stakeholder and client relationship management, • Program and project management for global validation initiatives, • Risk and issue management with mitigation planning, • Resource planning and capacity management, • Governance, reporting, and executive communication, • Budget awareness and delivery management xcskxlj • Cross-functional coordination across IT, QA, Business and Vendors Required Skills & Competencies • 10+ years of experience in Life Sciences CSV/CSA, • Exposure to cloud/SaaS validation, • Strong experience in enterprise systems (SAP S/4HANA, Veeva Vault, LIMS, QMS etc.), • understanding of SDLC and validation lifecycle, • Understanding on regulatory guidelines (GAMP 5, GxP, 21 CFR Part 11, EU Annex 11 etc.), • Experience in risk-based validation and CSA approach, • Experience working with US and European clients and regulated environments, • Strong documentation, communication, and leadership skills.

About Us JINGDONG Logistics (JD Logistics) is the logistics arm of JD.com and one of the world's leading technology-driven supply chain solutions providers. Leveraging advanced expertise in automation, intelligent logistics, and data-driven operations, we deliver end-to-end logistics solutions that help businesses grow while enhancing customer experience. Our capabilities span the entire supply chain, including warehousing, line-haul transportation, last-mile delivery, bulky goods logistics, cold chain solutions, and cross-border operations. Our mission is simple: to deliver speed, reliability, and operational excellence at every stage of the supply chain. The Mission & Core Scope • The Mission: Oversee the physical installation, testing, and continuous operational maintenance of all warehouse infrastructure, automation systems, and mechanical equipment to guarantee maximum uptime from Day One, • The Scope: You will manage technical contractors, supervise the deployment of racking, automated conveyor belts, and sorting systems, and implement the local preventative maintenance framework for the Madrid facilities Crucial Expectations & Performance Targets To provide a clear understanding of the accountability required, the successful candidate will be evaluated on the following key metrics during the initial 6 to 12 months: • Infrastructure Commissioning: Ensure all automated systems, sorters, scanning equipment, and physical structures are installed, tested, and legally certified strictly on schedule for the site launch, • Vendor & Contractor Management: Successfully supervise and audit third-party engineering contractors, ensuring all installations strictly adhere to agreed technical blueprints, budget constraints, and EU/Spanish industrial standards (Normas UNE / CE marking), • Equipment Reliability Architecture: Design and deploy a robust preventative and corrective maintenance schedule, minimizing operational downtime and maximizing the lifecycle of automated and mobile assets, • Technical Asset Compliance: Guarantee that 100% of the warehouse machinery, charging stations, and mechanical infrastructure meet local industrial safety and energy regulations Position Requirements • Greenfield Launch Expertise: You must have a verified engineering or technical background successfully managing facility setups, automation rollouts, or reliability maintenance engineering (RME) for a large-scale distribution center or manufacturing site launch, • Technical Background: A degree or advanced technical certification in Mechanical, Electrical, or Industrial Engineering, with deep knowledge of automated material handling systems (MHS) and PLC-driven environments, • Language Proficiency: Professional fluency in English and Spanish is mandatory to manage local technical contractors and align on technical engineering specifications with global HQ. Knowledge of Mandarin is a highly valued corporate asset, • Operational Agility: Complete flexibility to oversee technical operations during non-standard hours, test cycles, and emergency equipment interventions during the critical commissioning phase Diversity & Inclusion At JD Logistics, we are committed to building an inclusive workplace where everyone can th rive.We are proud to be an Equal Opportunity Employer. Employment decisions are made based on qualifications, merit, and business needs, regardless of race, ethnicity, gender, gender identity, sexual orientation, age, disability, religion, or any other characteristic protected by applicable law.Ready to Build the Future of Logis tics?Take the next step in your career and join one of the world's fastest-growing logistics compa nies.Apply today and help shape the future of intelligent logistics with JD Logistics.

At Quaker Houghton, we are experts in the development, production and application of industrial process fluids, lubricants and coatings for the manufacturing industry. We have been an integral part in the growth of the world's largest industrial and manufacturing companies from aerospace and automotive to primary metal and energy. Today, we have a global presence, with our corporate headquarters located in Conshohocken, PA. Quaker Houghton is a global publicly traded company with a unique collaborative culture that supports career growth for its colleagues and offers competitive compensation and benefit programs. Our people are our greatest strength. We are a global team of colleagues who collaborate to move forward together and exceed our customers' expectations. As a Customer Service Representative, you will play an essential role at the heart of our operations, helping to deliver an outstanding experience for our customers. What do we offer? • Immediate start date, • A fixed-term contract for 6 months, with potential to extend., • Flexible working arrangements, including remote working, with a preference for candidates located within reasonable proximity to one of our offices., • An international, collaborative and dynamic work environment, • QH University that offers continuous training tools for all seniority levels., • Wellbeing, Colleague Resource Groups & other attractive DEI programs., • Global Giving initiatives offering paid volunteering leave to dedicate to the cause of your choice., • Joining a team where supporting each other is part of the culture, in a company where customer success is our own. What will you do? Deliver an exceptional customer service experience by consistently providing high-quality support and exceeding customer expectations. You don't need to come from a chemicals or manufacturing background — we're open to candidates from other sectors such as logistics, FMCG, or similar industries. • Communicating with customers and colleagues across different countries., • Processing and managing customer orders., • Providing updates on order status, shipments, and deliveries., • Working closely with Supply Chain, Logistics, Production, and Sales teams., • Supporting quotation requests and customer enquiries., • Maintaining accurate customer records and documentation. What are we looking for? We're looking for enthusiastic and customer-focused individuals who enjoy working with people, solving problems, and learning new skills. Experience • Previous customer service, supply chain, or logistics experience is helpful but not essential., • We welcome early-career professionals, recent graduates, and anyone eager to learn and grow in a professional environment. Skills & Knowledge • Comfortable using Microsoft Office applications such as Outlook, Word, and Excel., • Experience with ERP systems is an advantage but not required – we will provide training., • Strong communication skills in English and German (written and spoken) are essential. What will help you succeed? • A genuine passion for delivering excellent customer service., • Strong communication and interpersonal skills., • A positive, proactive attitude and willingness to learn., • Good organizational skills and attention to detail., • Ability to collaborate effectively with others while also managing tasks independently., • Adaptability and a solution-focused mindset., • A commitment to safety, quality, and doing the right thing. Who are we? Quaker Houghton is the global leader in industrial process fluids, continually improving and innovating so the world's steel, aluminum, automotive, aircraft, machinery and industrial parts manufacturers can stay ahead in a changing world. Our chemists, engineers and industry experts partner with our customers to continually improve their operations so they can run even more efficiently, even more effectively, whatever comes next. Our values: Live Safe, Exceed Customer Expectations, Drive Results, Embrace Diversity, Do Great Things Together and Act with integrity. Our core values embody who we are as a company, guide our decisions and inspire us. Our commitment to these values, in words and actions, builds a safer, stronger Quaker Houghton. They are the fundamental beliefs that guide our internal conduct and our relationship with the outside world. Send us your application and FIND YOUR FUTURE! EEO: Quaker Houghton is committed to equal employment opportunities and a workplace free of discrimination. Applications are welcome from all qualified candidates regardless of gender, gender identity, age, disability, ethnic origin, religion, or sexual orientation. In line with the EU Pay Transparency Directive, the salary range for this role is disclosed before the interview to support transparency and consistency in our hiring process. Candidates will not be asked about their salary history. Our company uses a structured job level and salary band framework to support objective and consistent compensation decisions.

ph3Nature of the Tasks /h3 ul liArchitecture and design of systems, under the domains of Cloud architecture, Application architecture, Infrastructure architecture or Data architecture. /li liReview of the architecture of existing systems. /li liDesign and development of component architecture and building blocks. Analysis of requirements and modelling of Information Systems. /li liAnalysis of the integration possibilities of different information systems. Data analysis and data modelling. /li liCoordination of the implementation of the technical architecture. Technical interfacing between the project leaders and the developers. Production of architecture documents. /li liParticipation in technical working groups, progress meetings and meetings with the users. /li liAssistance in the analysis, testing, technical documentation, deployment, evaluation and reporting. /li /ul h3Knowledge And Skills /h3 ul liIn-depth knowledge of the techniques and practices related to the relevant architectural domain (Cloud, application, infrastructure, data). /li liIn-depth knowledge of Service Oriented Architecture. In depth knowledge of applications design. /li liIn depth knowledge of modelling tools. Good knowledge of Enterprise Architecture. Good knowledge of Relational DBMS. /li liGood knowledge of business process analysis. /li liKnowledge of interoperability technology (e.g. web services, message oriented middleware, service oriented bus). /li liKnowledge of software development methodologies (e.g. RUP, AGILE). Good redaction skills. /li liVery good knowledge of GIT. /li liAbility to give technical presentations. Ability to apply high quality standards. /li liAbility to cope with fast changing technologies used in application architecture and design. /li liAbility to participate in multi-lingual meetings, good communication skills. /li liCapability of working in a team. /li /ul h3Education And Experience /h3 ul liMinimum 13 years of relevant studies and/or experience after the secondary school. /li liMinimum 8 years of IT professional experience. /li liMinimum 4 years of experience in architecture and design of information systems. /li liMinimum 4 years of experience in development of information systems. /li liMinimum 4 years of experience with UML, BPMN or equivalent Business Process Analysis or modelling tool. /li /ul /p #J-18808-Ljbffr

pIt's a good feeling to know you're doing your best with purpose every day. At Artivion, we manufacture high-quality products and solutions for the treatment of aortic diseases. Together with surgeons worldwide, we save lives. In doing so, we rely on the strengths of each and every employee. Your strength counts, too: As an important link in the chain, you make a contribution to saving lives together with us. Bring your strengths and let us grow together. /ppbr/ppbWe are hiring a /b /ppbClinical Research Associate III – Home-Based in Spain (Spanish speaking candidates in France are also welcome) /b /ppbr/ppbYour Strength /b /ppbr/pulliMinimum of 4 years of advanced experience in clinical research monitoring /liliIn-depth knowledge of regulations and guidelines related to clinical trials involving human subjects (e.g., ISO 14155, GCP, MDR, EU, FDA) /liliAbility to independently manage 10–15 study sites from start-up through close-out /liliExcellent communication skills for site interaction, training, and issue resolution /liliStrong collaboration and mentorship abilities, with a passion for supporting and guiding junior team members /liliHands-on experience with monitoring systems, source data verification, and compliance tracking /liliStrong organizational skills with the ability to manage multiple priorities in a dynamic environment /liliWillingness to travel regularly for site visits and investigator meetings across France and Spain /liliBased in Spain (candidates from France may be considered in case a candidate lives nearby the Spain/France border and eager to do cross border monitoring) /liliFluent communication in English and Spanish (Catalan is preferred, French optional) /li /ulpbr/ppbYour Contribution /b /pulliIndependently manage all phases of clinical trial site activities, including site identification, initiation, monitoring, and close-out /liliConduct monitoring visits in accordance with study protocols, GCP, and applicable regulatory requirements /liliAct as the primary contact for investigational sites, ensuring compliance and providing ongoing support /liliBuild and maintain strong relationships with investigators, study coordinators, and site personnel /liliIdentify study risks, recommend solutions, and ensure timely resolution of site-related issues /liliPerform source data verification and data review to ensure patient safety, protocol compliance, and data integrity /liliConduct site training, initiation visits, and support audit and inspection readiness /liliCollaborate closely with Clinical Operations, Data Management, Medical Affairs, and other cross-functional teams /liliSupport investigator meetings, coordinator meetings, and deliver presentations or training sessions when required /liliMentor junior CRAs and contribute to process improvements and best practices /liliParticipate in CAPA activities, quality initiatives, audits, and continuous improvement efforts /li /ulpbr/ppbOur Strength /b /ppbr/pulliA mission-driven company focused on saving lives /liliInternational and collaborative MedTech environment /liliHybrid working model with flexibility /liliOpportunities for growth and professional development /liliInnovative products and meaningful clinical impact /li /ulpbr/ppbContact /b /ppApply now and join the Artivion team. We look forward to receiving your application documents in bEnglish /b through our online application system. /ppbBrian Russo /b /ppbr/ppT: /ppJOTEC GmbH, a wholly owned subsidiary of Artivion, Inc. /ppLotzenäcker 23, 72379 Hechingen /p pbr/p

OverviewThis position is posted by Jobgether on behalf of YLD. We are currently looking for a Contract QA Engineer in EU.As a Contract QA Engineer, you will play a crucial role in ensuring the quality and reliability of software applications by performing automated, manual, and exploratory testing. You will work closely with cross-functional teams to identify, report, and troubleshoot issues, helping to deliver robust and scalable solutions. This role offers the opportunity to contribute to complex Node.Js environments while developing testing frameworks and strategies. You will collaborate in a dynamic, remote-first environment, helping shape testing best practices and ensuring high-quality deliverables that meet both technical and business expectations.ResponsibilitiesDesign, implement, and maintain automated build, test, and release processesDevelop and maintain test automation frameworks and reusable test scriptsEvaluate product code against specifications and ensure functionality, reliability, and performanceCollaborate with QA engineers and cross-functional teams to define and improve testing strategies and plansReport bugs, troubleshoot issues, and ensure continuous improvement of product qualityConduct post-release and post-implementation testing to verify changesDrive adoption of tools, frameworks, and best practices to enhance testability and code qualityRequirementsProven experience as an Automation or QA Engineer, or in a similar roleHands-on experience in Node.Js environmentsFamiliarity with test automation tools (e.G., Playwright, Browser Stack) and performance/load testing tools (e.G., k6, JMeter)Knowledge of QA methodologies, Agile frameworks, and regression testingStrong analytical, problem-solving, and troubleshooting skillsExcellent organizational and communication skills, both verbal and writtenAbility to work in a dynamic, remote-first environment with a focus on client expectationsEnglish fluencyBenefitsCompetitive compensation for contract engagementFlexible working arrangements with remote-first setup across EUOpportunity to work with innovative teams and develop new skills in QA and software engineeringExposure to complex software systems and cutting-edge testing toolsCollaborative and ethical work environment with a focus on professional growthJob detailsSeniority level: Mid-Senior levelEmployment type: ContractJob function: Information TechnologyIndustries: Non-profit Organizations and Primary and Secondary Education

pTheWhiteam is seeking an experienced PMO Consultant to support large-scale transformation programmes. This role involves ensuring strong governance, effective coordination, and high-quality reporting across various workstreams. /ppThe ideal candidate will have 5-7 years of PMO experience, expertise in governance frameworks, and excellent communication skills. This position is remote (EU) and offers a rate of €42/hour. /p #J-18808-Ljbffr

Role: System Validation, Platform QualificationDesplácese hacia abajo para obtener una visión general completa de lo que requerirá este trabajo. ¿Es usted el candidato adecuado para esta oportunidad?Location: Spain(100% Remote)Client: InfosysSal: Market RangePermanent full-time positionRequirements and number of open positions3-5 years- 2 Positions in Open5-10 Years- 2 Positions in Open10+ years - 2 Positins in OpenRole OverviewWe are looking for a highly experienced Validation resource with 10+ years of experience in Computerized System Validation (CSV) within the Life Sciences domain. The candidate will lead end-to-end validation activities for enterprise-level software systems and manage teams, stakeholders, and delivery for global programs.Key Responsibilities- Lead end-to-end validation lifecycle (Planning, Risk Assessment, Testing, Release, Periodic Review)- Drive validation strategy for enterprise programs across regions (Europe/Global)- Manage validation teams, allocate work, and ensure timely delivery- Act as primary point of contact for client stakeholders and leadership- Lead governance, status reporting, and escalation management- Author and review validation deliverables (URS, FRS, IQ/OQ/PQ, RTM, Validation Report)- Ensure compliance with 21 CFR Part 11, EU Annex 11, Data Integrity (ALCOA+)- Manage quality processes (Deviation, CAPA, Change Control)- Support regulatory audits and inspection readiness- Mentor and coach junior resources, build capability within the team- Drive continuous improvement and standardization of validation processesManagerial Skills- Team leadership and people management- Stakeholder and client relationship management- Program and project management for global validation initiatives- Risk and issue management with mitigation planning- Resource planning and capacity management- Governance, reporting, and executive communication- Budget awareness and delivery management xhfqzwm - Cross-functional coordination across IT, QA, Business and VendorsRequired Skills & Competencies- 10+ years of experience in Life Sciences CSV/CSA- Exposure to cloud/SaaS validation- Strong experience in enterprise systems (SAP S/4HANA, Veeva Vault, LIMS, QMS etc.)- understanding of SDLC and validation lifecycle- Understanding on regulatory guidelines (GAMP 5, GxP, 21 CFR Part 11, EU Annex 11 etc.)- Experience in risk-based validation and CSA approach- Experience working with US and European clients and regulated environments- Strong documentation, communication, and leadership skills.

Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing Saa S companies in history, we surpassed $2 B in revenue in our last fiscal year with extensive growth potential ahead.At the heart of Veeva are our values: Do the Right Thing, Customer Success, Employee Success, and Speed. We're not just any public company – we made history in 2021 by becoming a public benefit corporation (PBC), legally bound to balancing the interests of customers, employees, society, and investors.As a Work Anywhere company, we support your flexibility to work from home or in the office, so you can thrive in your ideal environment.Join us in transforming the life sciences industry, committed to making a positive impact on its customers, employees, and communities.The RoleWe are looking for an experienced Senior Consultant with deep expertise in navigating customers through complex software implementation. Veeva’s Vault RIM suite is the industry’s only unified software solution that provides fully integrated regulatory information management (RIM) capabilities, including data and document management, submission publishing, and archival on a single cloud-based platform.As a key member of our Professional Services team, the Senior Consultant will be responsible for understanding our customers’ global regulatory needs, translating requirements into solution design, and defining global strategies for deploying our cloud-based solution for managing regulatory information across the enterprise.There is no work location requirement (remote position) within the EU/UK if a candidate is in close proximity to an airport and able to meet travel requirements. Qualified EU/UK based candidates are encouraged to apply.What You’ll DoLead software implementation projects at life sciences companies ranging from the world's largest pharmaceutical companies to emerging biotechsLead the solution design for implementation and use of the Vault Regulatory suite (Veeva Registrations, Veeva Submissions, Veeva Submissions Archive, Veeva Publishing)Lead configuration requirements workshops, design, prototype, configure, and document content solutionsProgram and project management, including resource planning, leading and motivating a cross-functional teamPrimary customer liaison managing communication between the project team, customer, and internal stakeholdersMentor project team and consultants, helping others improve their consulting skillsRequirements8+ years experience performing system implementations for life sciences or healthcare companies, either as a consultant, business or IT representativeIn-depth knowledge of drug development processes and regulatory submissions; including, Labeling, Submission Publishing and/or Viewing systemsProven ability to collaborate and communicate excellently with diverse stakeholders and ensure delivery to a high degree of satisfactionInfluential; experience leading teams through hard decisions and negotiating compromisesTechnical abilities and willingness to “roll up your sleeves” to design, configure and implement a RIM solutionExpert on life sciences compliance and computer systems validation requirementsAbility to work independently in a fast-paced environmentAbility to travel as required by the businessNice to HaveDirect experience with systems such as Veeva Vault, PAREXEL/ LIQUENT In Sight, CSC Regulatory Tracker, Aris Global Register, Open Text, Share Point, Documentum, First Doc/First Point, Next Docs, CARA, Salesforce, Workday, Oracle, SAP, Lorenz Docubridge, Extedo e CTD Manager, Master Control, Trackwise, other regulatory information management or submission publishing systems, nsulting experience, working with a major system integrator or software vendorPMP certificationExecution experience with Agile methodology and/or ACP CertificationSaa S/Cloud experienceFluency in one or more of the following languages: German, French, Spanish, ItalianVeeva’s headquarters is located in the San Francisco Bay Area with offices in more than 15 countries around the world.As an equal opportunity employer, Veeva is committed to fostering a culture of inclusion and growing a diverse workforce. Diversity makes us stronger. It comes in many forms. Gender, race, ethnicity, religion, politics, sexual orientation, age, disability and life experience shape us all into unique individuals. We value people for the individuals they are and the contributions they can bring to our teams.If you need assistance or accommodation due to a disability or special need when applying for a role or in our recruitment process, please contact us at talent_accommodations@.

¿Are you ready to take your next professional step?Bluetab an IBM Company, in Spain is calling!We are looking for Data & Cloud passionate professionals who want and have the necessary documentation to work in Europe.Working in Spain (Barcelona, Alicante, Bilbao, Madrid), you could have your cake and eat it; amazing Data and Cloud EMEA (International) projects and a fantastic lifestyle.We are ¡Great Place to Work & Best Work to Place!, known for being one of the best companies to work for in Spain.A very techie company which has led us to be the powerful arm of IBM in Data, Cloud, ML & AI. We help accelerate and optimize strategies in data and cloud platforms, taking full advantage of their architecture and development environments, for key companies in multiple industries.We offer the opportunity to work in environments with a high level of technological expertise in the Data & Cloud world; where you will be able to develop yourself personally and professionally, learn, train and share technological experiences where a philosophy of teamwork and collaboration is fostered.We are bluetaber, we love everything to do with technology, challenges and most of all People. We are restless, non-conformist, eager to learn more and we love nothing more than to take on a new technological challenge in all shapes and forms, with a fantastic team of professionals.We are looking for Data & Cloud Engineer world champions who love data, immersing themselves in the finer detail, analysis and technology.For these, we ask for the following:- Familiar with programming and experience in Python/PySpark or Scala/Spark- Experienced in a 100% Cloud environment (AWS/ Azure/ GCP)- Knowledge of Docker and Kubernetes is a plus.- Data analysis and generation of insights for either internal business areas or any other client.- A high level of English is highly desirable.- Knowledge of Spanish is an asset- Applicants must have a valid EU work permitWe work on Big Data architectures (AWS EMR with Spark) and horizontally scalable persistence layers in Cloud S3 system, deploying CI/CD S3 system, deploying CI/CD of infrastructure services with Terraform.We are working on the design and development of data integration processes with Python in Kubernetes or Databricks (Spark). Orchestration with DataFactory (Azure).We also work with Google Cloud Platform (GCP) and their own services such as BigQuery, Dataflow, Dataproc.Important:Applicants must have a valid EU work permitAnd now for the Good bit: Being a Bluetaber… ¿What can we offer?- Permanent contract and competitive salary according to position and experience.- Moving to Spain?¡Yes please! We will help you with your relocation and administrative formalities throughout the process. Can relocate to Spain from EU.- The sixty four million dollar question in the room. ¿Working from home? “Flexible telework Company”. Once in Spain, you will have access to our offices located in the centre of Madrid, Bilbao, Barcelona and Alicante with great transport links.- Flexible timetable start and finish, to suit your personal needs and reduced timetable on Fridays and during the summer (July and August)- 23 days holiday+ 2 bluetab days (Christmas Eve and New year’s eve)- Luncheon vouchers (11 euros per working per 8 hour working day) as a benefit over and above salary.- Medical Insurance and dental policy with extensive coverage as a benefit over and above salary- Entitlement to tax free transport and kindergarden care.- On going training plan based on platform gamification with rewards, up to 800 courses and official certifications- In addition, you will have Access to our Career Coach programme, designed to shadow you through your development and growth within Bluetab, with ongoing assessment and feedback.- ¡You will be in charge of your own growth!- Birthday gift card to the value of 50 euros.At Bluetab, we believe that diversity is enriching and as such, we wish to safeguard both inclusion and equal opportunities, for this reason Bluetab has an Equality Plan and Ethical Code which includes the above principles in order to guarantee non discrimination of our employees for questions of race, colour, nationality, social background, age, sex, marital status, sexual orientation, ideology, political leaning, religion or any other personal aspect whether it be physical or social.Bluetab is an IBM Company, but will remain the hiring entity. By proceeding with this application, you understand that Bluetab will share your personal information with other IBM affiliates involved in your recruitment process, wherever these are located. More Information on how IBM protects your personal information, including the safeguards in case of cross-border data transfer, are available here: https://www.Ibm.Com/careers/us-en/privacy-policy/If you are mad about technology and be part of an innovative environment, 100% techie, then Bluetab is for you.What are you waiting for?#J-18808-Ljbffr

ph3Cybersecurity IT Specialist, EU (remote) - International client /h3 pJob role: Cybersecurity IT Specialist, expertise in Splunk. /p h3Key knowledge required /h3 pSplunk. Minimum experience: 3 to 5 years. /p h3Studies required /h3 pTechnical Engineer. /p h3Language /h3 pEnglish (C1). /p h3Location /h3 pEU (remote). /p h3Description /h3 pWe are seeking a Cybersecurity IT Specialist with strong expertise in Splunk to join a multifunctional security operations team. The role focuses on SIEM monitoring, incident response (L1/L2), and support of security tools including endpoint, email, and vulnerability management platforms. The position requires 3–5 years of experience, a technical engineering background, and fluent English. Shift rotation and on‑call availability are required. /p h3Key responsibilities /h3 ul liMonitor, analyze, and triage security alerts using Splunk SIEM. /li liPerform L1/L2 incident response: investigation, containment, reporting, and ticket handling. /li liSupport EDR (Carbon Black), email security (Proofpoint), and vulnerability management (Tenable) operations. /li liDevelop and maintain detection use cases, playbooks, and log/source integrations. /li liExecute agent‑based and agentless vulnerability scans and coordinate remediation follow‑up. /li liCreate operational KPIs and contribute to written incident reports. /li liCollaborate with internal stakeholders during security events. /li /ul h3IT skills /h3 ul liSplunk SIEM (parsing, dashboards, alerting, use case development). /li liCarbon Black (EDR), Proofpoint (email security), Tenable (vulnerability scanning). /li liIncident response (L1/L2), alert triage, ticketing workflows, playbook documentation, KPI/report creation. /li /ul h3Rate /h3 p245-255€/day. /p /p #J-18808-Ljbffr

About Us Consulte la descripción del puesto a continuación. Si confía en que tiene las habilidades y la experiencia adecuadas, envíe su solicitud hoy mismo. JINGDONG Logistics (JD Logistics) is the logistics arm of and one of the world's leading technology-driven supply chain solutions providers. Leveraging advanced expertise in automation, intelligent logistics, and data-driven operations, we deliver end-to-end logistics solutions that help businesses grow while enhancing customer experience. Our capabilities span the entire supply chain, including warehousing, line-haul transportation, last-mile delivery, bulky goods logistics, cold chain solutions, and cross-border operations. Our mission is simple: to deliver speed, reliability, and operational excellence at every stage of the supply chain. The Mission & Core Scope • The Mission: Oversee the physical installation, testing, and continuous operational maintenance of all warehouse infrastructure, automation systems, and mechanical equipment to guarantee maximum uptime from Day One, • The Scope: You will manage technical contractors, supervise the deployment of racking, automated conveyor belts, and sorting systems, and implement the local preventative maintenance framework for the Madrid facilities Crucial Expectations & Performance Targets To provide a clear understanding of the accountability required, the successful candidate will be evaluated on the following key metrics during the initial 6 to 12 months: • Infrastructure Commissioning: Ensure all automated systems, sorters, scanning equipment, and physical structures are installed, tested, and legally certified strictly on schedule for the site launch, • Vendor & Contractor Management: Successfully supervise and audit third-party engineering contractors, ensuring all installations strictly adhere to agreed technical blueprints, budget constraints, and EU/Spanish industrial standards (Normas UNE / CE marking), • Equipment Reliability Architecture: Design and deploy a robust preventative and corrective maintenance schedule, minimizing operational downtime and maximizing the lifecycle of automated and mobile assets, • Technical Asset Compliance: Guarantee that 100% of the warehouse machinery, charging stations, and mechanical infrastructure meet local industrial safety and energy regulations Position Requirements • Greenfield Launch Expertise: You must have a verified engineering or technical background successfully managing facility setups, automation rollouts, or reliability maintenance engineering (RME) for a large-scale distribution center or manufacturing site launch, • Technical Background: A degree or advanced technical certification in Mechanical, Electrical, or Industrial Engineering, with deep knowledge of automated material handling systems (MHS) and PLC-driven environments, • Language Proficiency: Professional fluency in English and Spanish is mandatory to manage local technical contractors and align on technical engineering specifications with global HQ. Knowledge of Mandarin is a highly valued corporate asset, • Operational Agility: Complete flexibility to oversee technical operations during non-standard hours, test cycles, and emergency equipment interventions during the critical commissioning phase Diversity & Inclusion At JD Logistics, we are committed to building an inclusive workplace where everyone can th rive.We are proud to be an Equal Opportunity Employer. Employment decisions are made based on qualifications, merit, and business needs, regardless of race, ethnicity, gender, gender identity, sexual orientation, age, disability, religion, or any other characteristic protected by applicable law.Ready to Build the Future of Logis tics?Take the next step in your career and join one of the world's fastest-growing logistics compa nies. xkdbapo Apply today and help shape the future of intelligent logistics with JD Logistics.

ph3Overview /h3pDeveloper – Full Remote – EU Institutions role at TheWhiteam. (Internally repeated in the original content; refined to a single concise summary.) /ph3Responsibilities /h3ulliDevelop and maintain web or multi-tier applications. /liliImplement technical components and integrate them with existing systems. /liliTranslate user requirements into functional solutions. /liliParticipate in testing, prototyping, and technical documentation. /liliCollaborate with project teams in meetings and system deployments. /li /ulh3Knowledge And Skills /h3ulliDevelop and maintain web or multi-tier applications. /liliImplement technical components and integrate them with existing systems. /liliTranslate user requirements into functional solutions. /liliParticipate in testing, prototyping, and technical documentation. /liliCollaborate with project teams in meetings and system deployments. /li /ulh3Specific Expertise /h3ulliExperience in software development and application integration. /liliFamiliarity with web development frameworks and relational databases. /liliBasic knowledge of UML, BPMN, or similar modeling tools. /liliUnderstanding of Git and collaborative development workflows. /liliTeam-oriented, adaptable, and eager to learn new technologies. /liliDegree in Computer Science or related field. /liliFluency in English required. /li /ulh3Qualifications /h3ulliDegree in Computer Science or related field. /liliFluency in English required. /li /ulh3Seniority level /h3ulliEntry level /li /ulh3Employment type /h3ulliFull-time /li /ulh3Job function /h3ulliEngineering and Information Technology /li /ulh3Industries /h3ulliIT Services and IT Consulting /li /ul /p #J-18808-Ljbffr

¿Are you ready to take your next professional step? Lea atentamente toda la información sobre esta oportunidad y luego utilice el botón de solicitud de abajo para enviar su CV y su candidatura. Bluetab an IBM Company, in Spain is calling! We are looking for Data & Cloud passionate professionals who want and have the necessary documentation to work in Europe. Working in Spain (Barcelona, Alicante, Bilbao, Madrid), you could have your cake and eat it; amazing Data and Cloud EMEA (International) projects and a fantastic lifestyle. We are ¡Great Place to Work & Best Work to Place!, known for being one of the best companies to work for in Spain. A very techie company which has led us to be the powerful arm of IBM in Data, Cloud, ML & AI. We help accelerate and optimize strategies in data and cloud platforms, taking full advantage of their architecture and development environments, for key companies in multiple industries. We offer the opportunity to work in environments with a high level of technological expertise in the Data & Cloud world; where you will be able to develop yourself personally and professionally, learn, train and share technological experiences where a philosophy of teamwork and collaboration is fostered. We are bluetaber, we love everything to do with technology, challenges and most of all People. We are restless, non-conformist, eager to learn more and we love nothing more than to take on a new technological challenge in all shapes and forms, with a fantastic team of professionals. We are looking for Data & Cloud Engineer world champions who love data, immersing themselves in the finer detail, analysis and technology. For these, we ask for the following: • Familiar with programming and experience in Python/PySpark or Scala/Spark, • Experienced in a 100% Cloud environment (AWS/ Azure/ GCP), • Knowledge of Docker and Kubernetes is a plus., • Data analysis and generation of insights for either internal business areas or any other client., • A high level of English is highly desirable., • Knowledge of Spanish is an asset, • Applicants must have a valid EU work permit We work on Big Data architectures (AWS EMR with Spark) and horizontally scalable persistence layers in Cloud S3 system, deploying CI/CD S3 system, deploying CI/CD of infrastructure services with Terraform. We are working on the design and development of data integration processes with Python in Kubernetes or Databricks (Spark). Orchestration with DataFactory (Azure). We also work with Google Cloud Platform (GCP) and their own services such as BigQuery, Dataflow, Dataproc. Important: Applicants must have a valid EU work permit And now for the Good bit: Being a Bluetaber… ¿What can we offer? • Permanent contract and competitive salary according to position and experience., • Moving to Spain?¡Yes please! We will help you with your relocation and administrative formalities throughout the process. Can relocate to Spain from EU., • The sixty four million dollar question in the room. ¿Working from home? “Flexible telework Company”. Once in Spain, you will have access to our offices located in the centre of Madrid, Bilbao, Barcelona and Alicante with great transport links., • Flexible timetable start and finish, to suit your personal needs and reduced timetable on Fridays and during the summer (July and August), • 23 days holiday+ 2 bluetab days (Christmas Eve and New year’s eve), • Luncheon vouchers (11 euros per working per 8 hour working day) as a benefit over and above salary., • Medical Insurance and dental policy with extensive coverage as a benefit over and above salary, • Entitlement to tax free transport and kindergarden care., • On going training plan based on platform gamification with rewards, up to 800 courses and official certifications, • In addition, you will have Access to our Career Coach programme, designed to shadow you through your development and growth within Bluetab, with ongoing assessment and feedback., • ¡You will be in charge of your own growth!, • Birthday gift card to the value of 50 euros. At Bluetab, we believe that diversity is enriching and as such, we wish to safeguard both inclusion and equal opportunities, for this reason Bluetab has an Equality Plan and Ethical Code which includes the above principles in order to guarantee non discrimination of our employees for questions of race, colour, nationality, social background, age, sex, marital status, sexual orientation, ideology, political leaning, religion or any other personal aspect whether it be physical or social. Bluetab is an IBM Company, but will remain the hiring entity. xcskxlj By proceeding with this application, you understand that Bluetab will share your personal information with other IBM affiliates involved in your recruitment process, wherever these are located. More Information on how IBM protects your personal information, including the safeguards in case of cross-border data transfer, are available here: you are mad about technology and be part of an innovative environment, 100% techie, then Bluetab is for you. What are you waiting for? #J-18808-Ljbffr

JD Logistics is expanding its Madrid logistics network and seeks an Installation & Operations Manager to own the installation, testing, and ongoing maintenance of warehouse infrastructure, automation systems, and mechanical equipment from Day One. Las cualificaciones, habilidades y toda la experiencia relevante necesaria para este puesto se pueden encontrar en la descripción completa a continuación. You will manage technical contractors and supervise the deployment of racking, conveyors, and sorters. The role requires coordinating a local xcskxlj preventative maintenance program, ensuring safety, energy compliance, and alignment with EU/Spanish standards #J-18808-Ljbffr

Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing Saa S companies in history, we surpassed $2 B in revenue in our last fiscal year with extensive growth potential ahead.At the heart of Veeva are our values: Do the Right Thing, Customer Success, Employee Success, and Speed. We're not just any public company – we made history in 2021 by becoming a public benefit corporation (PBC), legally bound to balancing the interests of customers, employees, society, and investors.As a Work Anywhere company, we support your flexibility to work from home or in the office, so you can thrive in your ideal environment.Join us in transforming the life sciences industry, committed to making a positive impact on its customers, employees, and communities.The RoleWe are seeking talented individuals to join the Veeva Business Consulting group in R&D, a priority area for Veeva. We work with senior customer stakeholders, as the partner of choice for 85% of the top 20 Pharmaceutical companies, to define and realize the strategic value of Regulatory Affairs, Clinical Strategy & Operations as well as Quality and Safety (eg. Pharmacovigilance).As a Consultant, you will manage workstreams on consulting projects for Veeva customers in R&D – planning, organizing, and tracking all aspects of delivery. You will analyze problems, build insightful solutions, and develop close working relationships with customer stakeholders (through face-to-face discussions, workshops, email, etc.) to deliver demonstrable, sustainable value, at the forefront of digital and R&D innovation.Opportunities are available across Europe for this role as this is a remote position. There is no work location requirement if a candidate is in proximity to an airport and able to meet relevant travel requirements. Qualified candidates must be legally authorized to be employed in the EU (for EU locations, incl. Switzerland) and the UK (for UK-based candidates).What You’ll DoLead a workstream(s) in a project engagement: planning, organizing, and managing all aspects of delivery including scope, quality, resources, risk, and timelinesBe responsible for the end-to-end design, build, and delivery of deliverables that meet specific project goals and objectivesIdentify and proactively solve problems faced by the customerBe a primary client contact for operational project questions, developing the relationship through face-to-face discussions, workshops, phone, and email contactManage the work and priorities of Associate Consultants in your workstreamSupport and mentor Associates in developing skills and professional capabilitiesBuild trusted relationships with customer stakeholdersBring to your customers a good level of industry/ market/ functional insightsInput into business development opportunities and proposalsHelp develop and disseminate thought leadershipRequirementsBachelor's or Master’s degree and excellent academic record2+ years of consulting experienceStrong Life Sciences background with a keen interest in the R&D value chain or at minimum one or more of the following areas: Regulatory Affairs, Clinical Strategy, and Operations, Quality and SafetyGood understanding of technologies used in R&D and ideally Veeva’s platforms and solutions and how R&D consulting offerings can both leverage and support theseGood understanding of the business capabilities and drivers underpinning digital technology in health and life sciences and the market forces and trends driving industry changeProven analytical skills, able to quantitatively and qualitatively assess problems and communicate responses across a range of issuesA problem-solving mindset: anticipating issues early, analyzing and proactively finding solutionsDemonstrated leadership of others in the delivery of outcomesHighly efficient project management skillsSkilled in facilitating collaboration amongst team membersAble to work effectively with people at all levels in an organization and quickly establish credibilityHave a strong personal impact and ability to influence and persuade a range of stakeholdersAn effective communicator verbally and written, in English, and in the local office languageNice to HavePost-graduate-level qualification, Ph. D., MD, and/or MBAExperience with digital technologies – platforms, channels, analytics tools, apps, emerging technologyExperience working with Saa S solutionsFluency in other European languagesPerks & BenefitsHighly competitive remunerationOpportunity for rapid progressionHealth & wellness programs#Remote SpainBCRDVeeva’s headquarters is located in the San Francisco Bay Area with offices in more than 15 countries around the world.As an equal opportunity employer, Veeva is committed to fostering a culture of inclusion and growing a diverse workforce. Diversity makes us stronger. It comes in many forms. Gender, race, ethnicity, religion, politics, sexual orientation, age, disability and life experience shape us all into unique individuals. We value people for the individuals they are and the contributions they can bring to our teams.If you need assistance or accommodation due to a disability or special need when applying for a role or in our recruitment process, please contact us at talent_accommodations@.

OverviewAt Docplanner Group, we’re on a mission to help people live longer, healthier lives. As the world’s largest healthcare platform, we connect millions of patients with doctors across 13 countries. Our marketplaces, Saa S and AI tools simplify daily tasks and help doctors, clinics and hospitals work more efficiently so they can focus on caring for their patients. Learn more about our products here: pro.Doctoralia.EsWhy join us?Real impact – We help doctors help patients. Your work truly makes a difference.At scale, yet agile – 3,000+ employees, but still fast, flexible, and hands-on.Shape the future, sustain growth – Make a difference now and build for long-term success.Job DescriptionThe Risk & Compliance team ensures Docplanner meets regulatory requirements while supporting safe, scalable, and innovative healthcare solutions. As our products increasingly transition into medical device territory, regulatory compliance is a core enabler of our growth, trust and ability to operate globally.We are hiring aSenior Healthcare Regulatory Specialist (Sa MD)to join our global team. In this role, you will act as the Person Responsible for Regulatory Compliance (PRRC) under EU Medical Device Regulation (MDR), partnering closely with Product, Engineering, Machine Learning and Data, Customer Care and Legal teams to ensure our Software as a Medical Device (Sa MD) products meet regulatory requirements across Europe. You will play a key role in enabling Docplanner to operate safely, compliantly and at scale in an increasingly regulated digital healthcare environment.This is a new and highly impactful opportunity, where you will help build and strengthen our regulatory framework, directly supporting one of Docplanner’s core strategic priorities: EU MDR compliance and global expansion. You’ll gain exposure to innovative healthtech and AI-driven products, and work with cross-functional teams across multiple markets.How will you make an impact?EU MDR Compliance: Achieve mandatory Medical Device Regulation certification to maintain European market access.Support Global Certification Processes: Lead MDR certification and other accreditation (ISO, C5) processes across target jurisdictions to enable market expansion and continuance.Establish Compliant Governance Framework: Build robust governance systems that stakeholders and customers can trust, ensuring business integrity and regulatory adherence.Risk Mitigation & Business Protection: Prevent regulatory fines and reputational harm that could impact our ability to serve patients and healthcare providers.Process Optimization: Continuously assess and improve compliance processes to align with the dynamic needs of the increasingly regulated digital healthcare industry.QualificationsWhat will help you thrive?Strong knowledge of EU Medical Device Regulation (MDR), particularly in a Software as a Medical Device (Sa MD) context.Practical experience in medical device regulatory affairs and solid understanding of Quality Management Systems (QMS) and regulatory governance frameworks.Relevant academic background (law, medicine, pharmacy, engineering, or scientific field) or the equivalent hands-on experience in medical device regulatory/QMS experience.Experience with EUDAMED, CAPA systems, and post-market surveillance tools.Ability to manage cross-functional regulatory projects independently and work with multiple stakeholders.Strong communication skills with both internal teams and external regulatory authorities.Fluent in English; Spanish or other EU languages are a plus.Nice To HaveKnowledge of the EU AI Act.Familiarity with Agile / software development environments.The position is based in Spain and we are remote-friendly.Additional InformationWhat to Expect from Our Hiring ProcessIntro Chat– A first call with our Talent Partner to explore mutual fit around relevant skills, value alignment, and motivation.Business Case– A take-home exercise to understand how you approach real-life problems and regulatory scenarios, followed by a collaborative discussion with the hiring manager and team.Technical Interview– A deeper conversation about your background and experience with EU MDR and compliance, with the potential manager and team.Operational Interview– Discussion focused on operational fit, QMS integration and cross-functional collaboration.Final Interview– A final chat focused on cultural fit, values and strategic alignment.References & OfferWhy You’ll Love It HereGlobal Benefits– No matter where you are, you’ll have access to:Healthcare insurance – so you can focus on what matters.Wellness that works for you – from gym memberships to mental health support.Time off that counts – vacation, birthday, or a day to recharge.ESOP (Employee Share Option Plan) after 6 months with us.Local Perks– Depending on location, local benefits like meal vouchers, transport allowances, or extended parental leave.Career Growth– Opportunities to learn and develop through team or cross-functional projects.A Truly Global Team– Work with talented people from around the world in a diverse and inclusive environment.Flexibility That Works for You– Remote work and flexible hours; office hubs available in Barcelona, Warsaw, Curitiba, Rio de Janeiro, Mexico City, Bogotá, Munich, Rome or Bologna.Please note:We currently cannot sponsor visas for this position. You must have the legal right to work in your country of residence or the location of the role.What We Believe InAt Docplanner, our values guide everything we do:Focus on results –we’re here to make an impact.Think like an owner –take responsibility and drive outcomes.✂️ Keep it simple, keep it lean –smart solutions over complexity.Be respectful and radically honest –openness builds trust.Learn and be curious –growth is part of the job.Don’t just take our word for it—check out our Glassdoor to hear what our people say!We are committed to building a team that represents a variety of backgrounds, perspectives, and skills. We welcome applicants from all walks of life, and are dedicated to fostering an inclusive workplace where everyone feels valued and empowered to contribute.

A tech-driven company in Valencia is searching for an Off-site SEO Specialist. This role focuses on enhancing organic visibility through link-building and outreach initiatives, requiring at least 2 years of SEO experience. The ideal candidate should have strong communication skills, creativity, and a knack for relationship-building. Benefits include flexible working arrangements, wellness support, and professional development opportunities. Join a dynamic team and drive your career forward!#J-18808-Ljbffr

Senior Flight Dynamics Software EngineerWe are seeking a Senior Flight Dynamics Software Engineer who thrives in dynamic environments and enjoys working across disciplines—from coding and algorithm design to project leadership, customer interaction, and product strategy. You’ll help build and operate our Flight Dynamics System (FDS), integrate it with Mission Control (MCS), and collaborate with both commercial and institutional partners, including space agencies like ESA. This is a high-impact role with broad ownership. You’ll contribute to technical delivery, customer success, and strategic initiatives, including proposals and projects for space sustainability, SSA/SST, and mission operations.Tasks and ResponsibilitiesLead the end-to-end development of the Flight Dynamics System (FDS), including orbit determination, maneuver planning, and optimization for station-keeping and collision avoidance.Facilitate the integration of the FDS with the Mission Control System (MCS), ensuring seamless interoperability and mission-critical llaborate with satellite operators to capture operational requirements and translate them into system capabilities.Design and implement high-precision algorithms for orbit propagation, attitude dynamics, and trajectory optimization.Develop and maintain production‑grade software, using modern software engineering practices (version control, CI/CD, testing).Conduct verification and validation (V&V) campaigns using real-world datasets and operational scenarios.Provide technical leadership to the team and contribute to the strategic roadmap of our mission operations platform.Support customer deployments and provide expert guidance during mission preparation and execution.ProfileMust-haveM. Sc. or higher in Aerospace Engineering, Space Engineering, or a related field.Minimum 5 years of experience in the development and/or operation of Flight Dynamics, Mission Control, Space Traffic Management, Space Surveillance and Tracking, or space software.Strong theoretical and practical knowledge of orbital mechanics, astrodynamics, and spacecraft operations.Strong experience writing operational software in a compiled and high-level language (e.G., Python, Java, C++, Fortran, or similar).Demonstrated ability to lead complex technical projects and deliver high-quality software in a collaborative environment.Experience working directly with satellite operators or in operational satellite missions is mandatory.Based remote in Spain, with the ability to travel occasionally to our main offices in Braunschweig, Germany.Valid EU work authorization.Experience working with an international team, fully or partially remote.Nice-to-haveExperience with SSA/SST systems, sensor fusion, or catalog maintenance.Experience working with or for space agencies (e.G., ESA, DLR) or institutional missions.Familiarity with ground segment software, mission planning tools, and telemetry/telecommand workflows.Experience with microservices architecture, containerization (e.G., Docker), and cloud-based deployments.Knowledge of mission control systems, ground segment operations, or automated mission planning.Why us?With a lean hierarchy and small working groups, you define your own way of work including flexible work hours.Work on groundbreaking space sustainability challenges with a team of top-tier engineers and scientists.Enjoy technical freedom. Influence system architecture, research methodologies, and data integration approaches.Grow continuously with access to training budgets, industry conferences, and networking opportunities.Be part of a strong engineering culture, with regular knowledge-sharing sessions, technical deep dives, and innovation sprints.Great team spirit, with company-wide events such as monthly all‑hands lunches, and social activities like laser tag, dinners, and team‑building outings.About UsOKAPI: Orbits is at the forefront of space sustainability, addressing some of the most pressing challenges of the space industry: the growing problem of crowded orbital regimes, and the need for more efficient satellite operations. We’re providing end-to-end solutions that help various space industry players cover their Space Situation Awareness (SSA), and Space Traffic Management and Coordination (STM & STC) needs. We are committed to safeguarding space missions and access to space for all humanity. Join us on our mission.Last but not least, we would like to share with you that research shows that women areless likely to apply for a position unless they meet 100%of the listed requirements.Please know that if it’s your case — but you are passionate about space technology, building reliable software, and contributing to a more sustainable space environment — we strongly encourage you to apply.OKAPI: Orbits already brings together a highly diverse team, and we actively continue to strengthen this diversity which allows us to achieve higher performance and drive innovation.

About UsConsulte la descripción del puesto a continuación. Si confía en que tiene las habilidades y la experiencia adecuadas, envíe su solicitud hoy mismo.JINGDONG Logistics (JD Logistics) is the logistics arm of and one of the world's leading technology-driven supply chain solutions providers. Leveraging advanced expertise in automation, intelligent logistics, and data-driven operations, we deliver end-to-end logistics solutions that help businesses grow while enhancing customer experience.Our capabilities span the entire supply chain, including warehousing, line-haul transportation, last-mile delivery, bulky goods logistics, cold chain solutions, and cross-border operations. Our mission is simple: to deliver speed, reliability, and operational excellence at every stage of the supply chain.The Mission & Core ScopeThe Mission: Oversee the physical installation, testing, and continuous operational maintenance of all warehouse infrastructure, automation systems, and mechanical equipment to guarantee maximum uptime from Day OneThe Scope: You will manage technical contractors, supervise the deployment of racking, automated conveyor belts, and sorting systems, and implement the local preventative maintenance framework for the Madrid facilitiesCrucial Expectations & Performance TargetsTo provide a clear understanding of the accountability required, the successful candidate will be evaluated on the following key metrics during the initial 6 to 12 months:Infrastructure Commissioning: Ensure all automated systems, sorters, scanning equipment, and physical structures are installed, tested, and legally certified strictly on schedule for the site launchVendor & Contractor Management: Successfully supervise and audit third-party engineering contractors, ensuring all installations strictly adhere to agreed technical blueprints, budget constraints, and EU/Spanish industrial standards (Normas UNE / CE marking)Equipment Reliability Architecture: Design and deploy a robust preventative and corrective maintenance schedule, minimizing operational downtime and maximizing the lifecycle of automated and mobile assetsTechnical Asset Compliance: Guarantee that 100% of the warehouse machinery, charging stations, and mechanical infrastructure meet local industrial safety and energy regulationsPosition RequirementsGreenfield Launch Expertise: You must have a verified engineering or technical background successfully managing facility setups, automation rollouts, or reliability maintenance engineering (RME) for a large-scale distribution center or manufacturing site launchTechnical Background: A degree or advanced technical certification in Mechanical, Electrical, or Industrial Engineering, with deep knowledge of automated material handling systems (MHS) and PLC-driven environmentsLanguage Proficiency: Professional fluency in English and Spanish is mandatory to manage local technical contractors and align on technical engineering specifications with global HQ. Knowledge of Mandarin is a highly valued corporate assetOperational Agility: Complete flexibility to oversee technical operations during non-standard hours, test cycles, and emergency equipment interventions during the critical commissioning phaseDiversity & InclusionAt JD Logistics, we are committed to building an inclusive workplace where everyone can thrive.We are proud to be an Equal Opportunity Employer. Employment decisions are made based on qualifications, merit, and business needs, regardless of race, ethnicity, gender, gender identity, sexual orientation, age, disability, religion, or any other characteristic protected by applicablelaw.Ready to Build the Future of Logistics?Take the next step in your career and join one of the world's fastest-growing logistics companies. xhfqzwm Apply today and help shape the future of intelligent logistics with JD Logistics.

It's a good feeling to know you're doing your best with purpose every day. At Artivion, we manufacture high-quality products and solutions for the treatment of aortic diseases. Together with surgeons worldwide, we save lives. In doing so, we rely on the strengths of each and every employee. Your strength counts, too: As an important link in the chain, you make a contribution to saving lives together with us. Bring your strengths and let us grow together.¿Es este el puesto que está buscando? Si es así, siga leyendo para obtener más detalles y no olvide enviar su solicitud hoy mismo.We are hiring aClinical Research Associate III – Home-Based in Spain (Spanish speaking candidates in France are also welcome)Your StrengthMinimum of 4 years of advanced experience in clinical research monitoringIn-depth knowledge of regulations and guidelines related to clinical trials involving human subjects (e.G., ISO 14155, GCP, MDR, EU, FDA)Ability to independently manage 10–15 study sites from start-up through close-outExcellent communication skills for site interaction, training, and issue resolutionStrong collaboration and mentorship abilities, with a passion for supporting and guiding junior team membersHands-on experience with monitoring systems, source data verification, and compliance trackingStrong organizational skills with the ability to manage multiple priorities in a dynamic environmentWillingness to travel regularly for site visits and investigator meetings across France and SpainBased in Spain (candidates from France may be considered in case a candidate lives nearby the Spain/France border and eager to do cross border monitoring)Fluent communication in English and Spanish (Catalan is preferred, French optional)Your ContributionIndependently manage all phases of clinical trial site activities, including site identification, initiation, monitoring, and close-outConduct monitoring visits in accordance with study protocols, GCP, and applicable regulatory requirementsAct as the primary contact for investigational sites, ensuring compliance and providing ongoing supportBuild and maintain strong relationships with investigators, study coordinators, and site personnelIdentify study risks, recommend solutions, and ensure timely resolution of site-related issuesPerform source data verification and data review to ensure patient safety, protocol compliance, and data integrityConduct site training, initiation visits, and support audit and inspection readinessCollaborate closely with Clinical Operations, Data Management, Medical Affairs, and other cross-functional teamsSupport investigator meetings, coordinator meetings, and deliver presentations or training sessions when requiredMentor junior CRAs and contribute to process improvements and best practicesParticipate in CAPA activities, quality initiatives, audits, and continuous improvement effortsOur StrengthA mission-driven company focused on saving livesInternational and collaborative MedTech environmentHybrid working model with flexibilityOpportunities for growth and professional developmentInnovative products and meaningful clinical impactContactApply now and join the Artivion team. xhfqzwm We look forward to receiving your application documents in English through our online application system.Brian RussoT: JOTEC GmbH, a wholly owned subsidiary of Artivion, Inc.Lotzenäcker 23, 72379 Hechingen

It's a good feeling to know you're doing your best with purpose every day. At Artivion, we manufacture high-quality products and solutions for the treatment of aortic diseases. Together with surgeons worldwide, we save lives. In doing so, we rely on the strengths of each and every employee. Your strength counts, too: As an important link in the chain, you make a contribution to saving lives together with us. Bring your strengths and let us grow together. We are hiring a Clinical Research Associate III – Home-Based in Spain (Spanish speaking candidates in France are also welcome) Your Strength • Minimum of 4 years of advanced experience in clinical research monitoring, • In-depth knowledge of regulations and guidelines related to clinical trials involving human subjects (e.g., ISO 14155, GCP, MDR, EU, FDA), • Ability to independently manage 10–15 study sites from start-up through close-out, • Excellent communication skills for site interaction, training, and issue resolution, • Strong collaboration and mentorship abilities, with a passion for supporting and guiding junior team members, • Hands-on experience with monitoring systems, source data verification, and compliance tracking, • Strong organizational skills with the ability to manage multiple priorities in a dynamic environment, • Willingness to travel regularly for site visits and investigator meetings across France and Spain, • Based in Spain (candidates from France may be considered in case a candidate lives nearby the Spain/France border and eager to do cross border monitoring), • Fluent communication in English and Spanish (Catalan is preferred, French optional) Your Contribution • Independently manage all phases of clinical trial site activities, including site identification, initiation, monitoring, and close-out, • Conduct monitoring visits in accordance with study protocols, GCP, and applicable regulatory requirements, • Act as the primary contact for investigational sites, ensuring compliance and providing ongoing support, • Build and maintain strong relationships with investigators, study coordinators, and site personnel, • Identify study risks, recommend solutions, and ensure timely resolution of site-related issues, • Perform source data verification and data review to ensure patient safety, protocol compliance, and data integrity, • Conduct site training, initiation visits, and support audit and inspection readiness, • Collaborate closely with Clinical Operations, Data Management, Medical Affairs, and other cross-functional teams, • Support investigator meetings, coordinator meetings, and deliver presentations or training sessions when required, • Mentor junior CRAs and contribute to process improvements and best practices, • Participate in CAPA activities, quality initiatives, audits, and continuous improvement efforts Our Strength • A mission-driven company focused on saving lives, • International and collaborative MedTech environment, • Hybrid working model with flexibility, • Opportunities for growth and professional development, • Innovative products and meaningful clinical impact Contact Apply now and join the Artivion team. We look forward to receiving your application documents in English through our online application system. Brian Russo T: +41 435 08 39 01 JOTEC GmbH, a wholly owned subsidiary of Artivion, Inc. Lotzenäcker 23, 72379 Hechingen www.artivion.com

Madrid, Barcelona or Bilbao Spain (On-Site) 75% travel requirement within Spain Todas las habilidades, cualificaciones y experiencia relevantes que necesitará un candidato seleccionado se enumeran en la siguiente descripción. Thermal Works LLC has an exciting opportunity for a Field Service Technician to join our team, working directly with the Thermal Works team as well as local contractors, focusing on Startup/Commissioning and Service for all Thermal Works equipment. We are looking for someone who is a detail-oriented individual that is goal oriented with a foundational knowledge in HVAC. This individual should have good written and verbal communication skills. The Field Service Technician needs to be agile, professional, trustworthy with confidential information, and comfortable in a rapidly changing environment. The right person can work equally as well independently as with a team. Thermal Works values efficiency and strives to maintain smooth operations. Our primary focus is on providing an integrated cooling system for data centers and commercial buildings that dramatically reduces the energy demand, water consumption and cost of cooling. It transforms the economics and eco-metrics of commercial cooling with zero water solutions that outperform air- and water-cooled systems in any climate. Thermal Works solutions are sustainable and cutting‑edge. For that reason, we are highly selective about the people we bring on board because our work depends on it. Change and progress happen quickly, and we must be able to trust one another to be honest, communicative, reliable, and self‑motivated. We seek ultra‑creatives and superstar performers with a sense of humility and a hunger to make a positive impact in the world. We offer flexibility and endless growth opportunities to those who can harness their skills and talents and identify how and where to use them to add value. Thermal Works is one of several “inspired infrastructure” companies that work collaboratively under our parent company, Endeavour Energy, LLC. At the heart of this ecosystem is a diverse group of bright, passionate, dedicated people, working together to make a real difference for people and the planet. Thermal Works is looking for someone to join our team to help us move the needle towards sustainable change. Are you ready to join the journey? Key Responsibilities • Participate in a comprehensive training program at Thermal Works’ U.S. headquarters., • Manage Preventive Maintenance and Service schedules., • Perform on‑site quality Control for the installation of Thermal Works products., • Perform all preventative maintenance and service needs for clients., • Be available to take emergency issues when on call., • Monitor service software closely to ensure services are met on a timely schedule., • Collaboration with different departments within the company for product development and improvement., • Provide technical support for troubleshooting and repair of thermal works equipment., • 75% travel requirement within Spain. Skills & Requirements • F‑Gas Category I Certification (in accordance with EC Regulation No. 517/2014) is required for handling fluorinated gases., • 3–5 years of hands‑on experience in mechanical systems for mission‑critical infrastructure, including data centers, healthcare, or industrial facilities., • Must have experience with chillers and CRAH (Computer Room Air Handler) units, encompassing installation, commissioning, preventive maintenance, and troubleshooting., • Familiarity with EU safety standards, pressure equipment directives (PED), and EN 378 refrigeration safety norms., • Capable of performing diagnostics, repairs, and system optimizations in live environments. Specific Skills / Abilities • Baseline circuit analysis and troubleshooting of electrical components., • Knowledge of hydronic systems., • Ability to effectively troubleshoot HVAC systems., • Understand refrigeration theory as well as hands‑on applied sciences., • Good written and verbal communication skills with an emphasis on customer service., • Fluent in English and Spanish (additional European languages are a strong plus)., • Ability to read drawings at a basic level., • Able to lift up to 50 lbs. continuously throughout the day. Great Place to Work A fast‑paced, entrepreneurial culture focused on innovation. A flexible, autonomous work environment. A culture of respect, learning, and excellence. Experienced, highly talented experts as team peers. Growth and travel opportunities. A team of change‑makers having a significant impact on people and the planet. About Our Parent Company Endeavour is the main hub—a self‑sustaining incubation platform for innovation—within a larger ecosystem focused on sustainable infrastructure. It provides the space, time, and all necessary resources to take advanced technologies from ideation through development to launch. Every day we are helping innovators to develop and launch global solutions to tackle global challenges, which is no easy task. Our teams work extremely hard because we all believe in Endeavour’s mission: to guarantee clean water and renewable energy to everyone, everywhere. We are working hard to decentralize infrastructure and deploy innovative energy, water, and waste treatment solutions that are more sustainable and more profitable than those currently in existence. Our team of passionate change‑makers want to leave the world better than the way we found it. Endeavour prides itself on hiring talented, highly motivated people because that’s what our mission requires. There is a strong sense of camaraderie between good‑natured people who bring their A‑game to work, every day, to make a difference. To work at Endeavour is to know that you are part of something special—something bigger than yourself. Today, we’re deploying solutions that are immediately scalable and profitable, including EV charging, data center cooling, and waste to fuel systems. As we look to the future, Endeavour intends to remain at the forefront of innovation, taking on grander challenges based on the needs of our clients and of local economies. xcskxlj We hope that our Sustainable Habitat for Innovation towards a Purpose (SHIP) will be a model that inspires people and businesses to join the journey so that together we can combine the best of what technology and the natural world can offer to ensure a regenerative/sustainable world for generations to come. Position Details • Position: Field Service Technician, • Full‑time or Part‑Time: Full‑time, • Reports to: Field Deployment and Commissioning Manager, • Location: Madrid, Barcelona or Bilbao Spain (On‑Site) 75% travel requirement within Spain #J-18808-Ljbffr

ph3Cybersecurity IT Specialist, EU (remote) - International client /h3 h3Job role: /h3 pCybersecurity IT Specialist, expertise in Splunk. /p h3Key knowledge required: /h3 pSplunk. Minimum experience: 3 to 5 years. /p h3Studies required: /h3 pTechnical Engineer. /p h3Language: /h3 pEnglish (C1). /p h3Location: /h3 pEU (remote). /p h3Description: /h3 pWe are seeking a Cybersecurity IT Specialist with strong expertise in Splunk to join a multifunctional security operations team. The role focuses on SIEM monitoring, incident response (L1/L2), and support of security tools including endpoint, email, and vulnerability management platforms. The position requires 3–5 years of experience, a technical engineering background, and fluent English. Shift rotation and on‑call availability are required. /p h3Key responsibilities: /h3 ul liMonitor, analyze, and triage security alerts using Splunk SIEM. /li liPerform L1/L2 incident response: investigation, containment, reporting, and ticket handling. /li liSupport EDR (Carbon Black), email security (Proofpoint), and vulnerability management (Tenable) operations. /li liDevelop and maintain detection use cases, playbooks, and log/source integrations. /li liExecute agent‑based and agentless vulnerability scans and coordinate remediation follow‑up. /li liCreate operational KPIs and contribute to written incident reports. /li liCollaborate with internal stakeholders during security events. /li /ul h3IT skills: /h3 ul liSplunk SIEM (parsing, dashboards, alerting, use case development). /li liCarbon Black (EDR), Proofpoint (email security), Tenable (vulnerability scanning). /li liIncident response (L1/L2), alert triage, ticketing workflows, playbook documentation, KPI/report creation. /li liTechnical engineering degree, 3–5 years of experience, English fluency, shift rotation, on‑call duties. /li /ul h3Rate: /h3 ul li245-255€/day. /li /ul /p #J-18808-Ljbffr

ph3bDescripción del empleo /b /h3 pFanox, parte de Wabtec Corporation, tiene su sede en Derio (Bizkaia) y diseña y fabrica relés electrónicos de protección y control para aplicaciones de Media Tensión y Baja Tensión. /p pComo Ingeniero/a de Protecciones, formarás parte del área de Aplicación, colaborando estrechamente con el responsable del área y el equipo para garantizar que los equipos diseñados en Fanox estén correctamente validados y funcionando de forma óptima, asegurando que cubren las necesidades del mercado. /p h3b¿Cómo marcarás la diferencia? /b /h3 pContribuirás a asegurar la calidad y fiabilidad de nuestros productos mediante la validación técnica de equipos y el soporte especializado, garantizando que las soluciones de protección cumplen con los estándares y expectativas del cliente. /p h3b¿Cómo será tu día a día? /b /h3 ul liValidación de equipos mediante pruebas funcionales, análisis de fallos y operación de equipos. /li liParticipación en procesos de homologación. /li liImpartición de cursos y seminarios técnicos a nivel nacional e internacional. /li liRevisión de especificaciones técnicas de cliente. /li liSoporte técnico interno y externo. /li liElaboración y actualización de documentación técnica. /li /ul h3b¿Qué queremos saber sobre ti? /b /h3 h3bFormación y base técnica /b /h3 ul liExtinta Ingeniería Industrial (Intensificación eléctrica) o Máster en Ingeniería Industrial (especialidad eléctrica o automática). /li /ul h3bExperiencia profesional /b /h3 ul liMínimo 5 años de experiencia en el área de protecciones eléctricas. /li /ul h3bConocimientos técnicos valorados /b /h3 ul liProtecciones eléctricas y relés de protección. /li liRed eléctrica y topología de red. /li liPruebas con maletas de inyección (tipo OMICRON, SVERKER, FREJA, etc.). /li /ul h3bCompetencias clave /b /h3 ul liToma de decisiones y resolución de problemas. /li liAlta capacidad de aprendizaje. /li liCapacidad de comunicación oral y escrita. /li /ul h3bIdiomas /b /h3 ul liEspañol: nivel fluido. /li liInglés: nivel alto (oral y escrito). /li /ul h3b¿Qué ofrecemos? /b /h3 ul liFlexibilidad horaria. /li liJornada intensiva los viernes y en verano. /li liMedidas de conciliación para el equilibrio vida personal‑profesional. /li /ul pLegal authorization to work in EU is required. We will not sponsor individuals for employment visas, now or in the future, for this job opening. /p /p #J-18808-Ljbffr

10x Team is seeking an experienced Identity & Access Management (IAM) Consultant to train AI systems with real-world IAM expertise. This freelance role is remote (EU/UK) and requires 8–20 hours per week on a project-based basis.You will review AI outputs, contribute case studies, and provide structured feedback on access control, identity governance, and regulatory compliance (GDPR, SOX). Ideal candidates are based in the EU or UK with strong analytical skills.

ppFanox, parte de Wabtec Corporation, tiene su sede en Derio (Bizkaia) y diseña y fabrica relés electrónicos de protección y control para aplicaciones de Media Tensión y Baja Tensión. /p pComo Ingeniero/a de Protecciones, formarás parte del área de Aplicación, colaborando estrechamente con el responsable del área y el equipo para garantizar que los equipos diseñados en Fanox estén correctamente validados y funcionando de forma óptima, asegurando que cubren las necesidades del mercado. /p h3¿Cómo marcarás la diferencia? /h3 pContribuirás a asegurar la calidad y fiabilidad de nuestros productos mediante la validación técnica de equipos y el soporte especializado, garantizando que las soluciones de protección cumplen con los estándares y expectativas del cliente. /p h3¿Cómo será tu día a día? /h3 ul liValidación de equipos mediante pruebas funcionales, análisis de fallos y operación de equipos. /li liParticipación en procesos de homologación. /li liImpartición de cursos y seminarios técnicos a nivel nacional e internacional. /li liRevisión de especificaciones técnicas de cliente. /li liSoporte técnico interno y externo. /li liElaboración y actualización de documentación técnica. /li /ul h3¿Qué queremos saber sobre ti? /h3 h3Formación y base técnica /h3 pExtinta Ingeniería Industrial (Intensificación eléctrica) o Máster en Ingeniería Industrial (especialidad eléctrica o automática). /p h3Experiencia profesional /h3 pMínimo 5 años de experiencia en el área de protecciones eléctricas. /p h3Conocimientos técnicos valorados: /h3 ul liProtecciones eléctricas y relés de protección. /li liRed eléctrica y topología de red. /li liPruebas con maletas de inyección (tipo OMICRON, SVERKER, FREJA, etc.) /li /ul h3Competencias clave /h3 ul liToma de decisiones y resolución de problemas. /li liAlta capacidad de aprendizaje. /li liCapacidad de comunicación oral y escrita. /li /ul h3Idiomas /h3 ul liEspañol: nivel fluido /li liInglés: nivel alto (oral y escrito) /li /ul h3¿Qué ofrecemos? /h3 ul liFlexibilidad horaria /li liJornada intensiva los viernes y en verano /li liMedidas de conciliación para el equilibrio vida personal‑profesional /li /ul pLegal authorization to work in EU is required. We will not sponsor individuals for employment visas, now or in the future, for this job opening. /p /p #J-18808-Ljbffr

pThe Whiteam seeks a senior Delivery Lead to drive end-to-end infrastructure refresh initiatives in a remote EU setting. You will coordinate with DXC and business units, define plans, manage risks, and ensure on-time, within-budget delivery across distributed teams. /ppCandidates must have 5+ years of relevant experience and a Bachelor’s Degree, with English at C1 level mandatory. The role emphasizes governance, financial controls, and high-quality documentation. #J-18808-Ljbffr /p

About the role ¿Es este el siguiente paso en su carrera? Descubra si es el candidato adecuado leyendo la descripción completa a continuación. We’re hiring a Conversion Rate Optimization (CRO) Manager to own the experimentation program that turns our paid traffic into signups, activations, and revenue. This role owns strategy and execution across the on‑site funnel—from the marketing site and landing pages to signup and partnering with onboarding—and is expected to find compounding conversion gains through a disciplined, data‑driven testing program. The ideal candidate is equally comfortable with the strategy and the execution: forming sharp hypotheses, designing statistically sound tests, building and QA’ing variants, reading results without fooling themselves, and engineering skills to build on‑page experiences. You obsess over funnel friction, statistical rigor, and velocity, and you know how to build an experimentation roadmap that ships. This role is highly cross‑functional and will partner closely with design, engineering, copy, performance marketing, lifecycle, and product to drive impact. What you will do Own the CRO strategy and experimentation roadmap across the marketing site, landing pages, and signup/onboarding funnels Form hypotheses from analytics, session data, and user research; prioritize tests by expected impact and effort Design, build, QA, and launch A/B and multivariate tests; ensure results are statistically sound Partner with design, engineering, and copy to spec and ship high‑quality variants quickly Analyze results, document learnings, and turn wins into durable improvements across the funnel Instrument funnel analytics and tracking so conversion impact is measurable end‑to‑end Align on‑site conversion with paid and lifecycle traffic in partnership with performance and lifecycle marketing Raise experimentation velocity and rigor as the program scales Requirements Proven track record owning a CRO/experimentation program that delivered measurable conversion and revenue gains Hands‑on expertise with A/B testing and CRO tools (Optimizely, VWO, Google Optimize successors, Statsig, GrowthBook, or similar), web analytics (GA4, Amplitude, Mixpanel, or similar), and front‑end development (HTML, CSS, and JavaScript) Strong analytical rigor—you understand statistical significance, sample size, and how to avoid false positives without a second opinion Experience optimizing signup, onboarding, and landing‑page funnels for both self‑serve and lead‑gen motions Comfortable working closely with design, engineering, and copy to ship high‑quality test variants Clear communicator who can turn data into decisions and bring the team along You thrive in scrappy, high‑ownership environments and are confident building a program from the ground up Bonus Experience with server‑side testing or feature‑flag‑based experimentation Experience marketing to technical audiences (e.g., developers, APIs, infrastructure) Experience standing up experimentation infrastructure or collaborating with data/BI teams Growth potential We believe in hiring the best talent in the world to make an impact in the right role at the right time. At ElevenLabs, strong performance creates opportunities for growth. xcskxlj Here are some of the career paths you can expect after excelling in this role: Lead the experimentation function across the full funnel as the team scales Expand into broader growth or growth‑product leadership Move into full‑funnel growth strategy or a channel‑owner leadership role Location This role is remote‑first, so it can be executed from anywhere in NA and EU. If you prefer, you can work from our offices in Dublin, London, New York, and Warsaw. #J-18808-Ljbffr

ph3Project Manager – Full Remote – EU Institutions /h3pGet AI-powered advice on this job and more exclusive features. /ph3Responsibilities /h3ulliLead planning, execution, and delivery of technology projects. /liliCoordinate cross-functional teams and manage project timelines, budgets, and risks. /liliCommunicate effectively with stakeholders and senior leadership. /liliMaintain clear documentation and ensure alignment with compliance and governance standards. /liliApply Agile or hybrid methodologies to drive project success. /li /ulh3Qualifications /h3ulliLead planning, execution, and delivery of technology projects. /liliCoordinate cross-functional teams and manage project timelines, budgets, and risks. /liliCommunicate effectively with stakeholders and senior leadership. /liliMaintain clear documentation and ensure alignment with compliance and governance standards. /liliApply Agile or hybrid methodologies to drive project success. /liliProficiency with tools like Jira, Confluence, or MS Project. /liliExcellent communication, organization, and problem-solving skills. /liliStrong understanding of IT systems or software delivery lifecycles. /liliFluent in English (written and spoken). /lili3+ years of experience in technology project management. /liliRelevant certifications (PMP, Scrum, PRINCE2) are a plus /liliPractical knowledge of quality standards linked to software development (e.g. ISO 10006:2003). /li /ulh3Seniority level /h3ulliMid-Senior level /li /ulh3Employment type /h3ulliFull-time /li /ulh3Job function /h3ulliProject Management and Information Technology /li /ulh3Industries /h3ulliIT Services and IT Consulting /li /ul /p #J-18808-Ljbffr

10x Team is looking for a Freelance VP Sales AI Trainer to enhance AI-generated sales content and strategies. In this role, you will assess the accuracy and relevance of AI outputs while leveraging your sales expertise to shape the future of AI in real-world scenarios.This is a flexible, project-based role that requires 8 to 20 hours of work per week. Ideal candidates will be senior sales leaders based in the EU or UK.

It's a good feeling to know you're doing your best with purpose every day. At Artivion, we manufacture high-quality products and solutions for the treatment of aortic diseases. Together with surgeons worldwide, we save lives. In doing so, we rely on the strengths of each and every employee. Your strength counts, too: As an important link in the chain, you make a contribution to saving lives together with us. Bring your strengths and let us grow together. We are hiring a Clinical Research Associate III – Home-Based in Spain (Spanish speaking candidates in France are also welcome) Your Strength • Minimum of 4 years of advanced experience in clinical research monitoring, • In-depth knowledge of regulations and guidelines related to clinical trials involving human subjects (e.g., ISO 14155, GCP, MDR, EU, FDA), • Ability to independently manage 10–15 study sites from start-up through close-out, • Excellent communication skills for site interaction, training, and issue resolution, • Strong collaboration and mentorship abilities, with a passion for supporting and guiding junior team members, • Hands-on experience with monitoring systems, source data verification, and compliance tracking, • Strong organizational skills with the ability to manage multiple priorities in a dynamic environment, • Willingness to travel regularly for site visits and investigator meetings across France and Spain, • Based in Spain (candidates from France may be considered in case a candidate lives nearby the Spain/France border and eager to do cross border monitoring), • Fluent communication in English and Spanish (Catalan is preferred, French optional) Your Contribution • Independently manage all phases of clinical trial site activities, including site identification, initiation, monitoring, and close-out, • Conduct monitoring visits in accordance with study protocols, GCP, and applicable regulatory requirements, • Act as the primary contact for investigational sites, ensuring compliance and providing ongoing support, • Build and maintain strong relationships with investigators, study coordinators, and site personnel, • Identify study risks, recommend solutions, and ensure timely resolution of site-related issues, • Perform source data verification and data review to ensure patient safety, protocol compliance, and data integrity, • Conduct site training, initiation visits, and support audit and inspection readiness, • Collaborate closely with Clinical Operations, Data Management, Medical Affairs, and other cross-functional teams, • Support investigator meetings, coordinator meetings, and deliver presentations or training sessions when required, • Mentor junior CRAs and contribute to process improvements and best practices, • Participate in CAPA activities, quality initiatives, audits, and continuous improvement efforts Our Strength • A mission-driven company focused on saving lives, • International and collaborative MedTech environment, • Hybrid working model with flexibility, • Opportunities for growth and professional development, • Innovative products and meaningful clinical impact Contact Apply now and join the Artivion team. We look forward to receiving your application documents in English through our online application system. Brian Russo T: +41 435 08 39 01 JOTEC GmbH, a wholly owned subsidiary of Artivion, Inc. Lotzenäcker 23, 72379 Hechingen www.artivion.com

Territory includes but not limited to: All of EU countries as needed The Regional Medical Director (RMD) is an integral member of the metabolic/obesity clinical sciences group, who assists and extends Clinical Sciences across the metabolic portfolio on assigned studies at the regional level. Site engagement and training o Retraining as needed (e.g., Meeting with potential sites, in collaboration with CTL, to discuss the program/assess of their interest o Patient recruitment issues (ongoing oversight): Meeting with sites, in collaboration with CTL, to help understand the hurdles with recruitment at their site and trouble shooting ~ o Helping address site medical/clinical questions as a first line for those questions that are straightforward or previously addressed or to help coordinate a response with the Medical Director for those that are not straightforward/new  This includes referencing and updating the FAQ, as applicable  Medical Director should always be copied on the email correspondence for oversight ~ o Helping site understand what is needed to close a medical query if there is a misunderstanding from the site regarding what is needed  Feedback should also be provided to the study team if the query text could be improved for clarity Ensuring that all information has been gathered as expected (i.e., in collaboration with the CRA, if additional support is needed during escalation process  o In collaboration with the CTL, retrain the site, to prevent future deviations/address any misunderstandings by the site ~ o Helping to ensure that the site has followed up with patients in the event of lost to follow-up / all appropriate steps have been taken (in collaboration with the CTL) and that any protocol specific requirements have been met ~ o For instance, in PNH studies, help to ensure that all LDH values that are not done/unable to be performed are rapidly chased to ensure a repeat is done as quickly as possible, in collaboration with the CRA/CTL o For other studies, may require help in working with site to obtain any key missing assessments (eg, images, PK samples, biomarker samples), in collaboration with the CRA/CTL ~ Laboratory reference range o In collaboration with the CRA, ensure that the laboratory reference ranges are provided for local laboratory data ~ The global medical director can be pulled in if the issue cannot be easily resolved Weekly meetings with medical director (if possible) or weekly communication with medical director, at a minimum May provide clinical assistance and feedback on PI interest in proposed studies at the local level Qualifications and Experience: ~ MD PhD, or PharmD; 8+ years of industry clinical development experience ~ Expertise in clinical trials and clinical development ~ Strong understanding of the Metabolic/Obesity clinical research landscape and implementation and conduct of these clinical trials ~ Demonstrated ability to work well in cross functional and geographically diverse teams ~ Cross cultural awareness and fluent in the local language of primary country assignment in addition to English ~ Computer skills including Excel, Word, and PowerPoint ~ A willingness to travel up to 65%, which may include local, regional and international travel ~ Valid driver's license

10x Team is seeking freelance Science/Bio/Health/Aviation researchers to help train AI. Roles are remote (EU/UK) and require 8–20 hours per week, with flexible, project-based assignments.Review AI-generated content for accuracy, develop real-world scenarios, and provide clear, structured feedback to improve AI reasoning in biology, medicine, public health, physics, and aviation domains.

Updated: 07 July 2026Freelance | 8–20 hrs/week | Remote (EU/UK)Are you an experienced specialist in e IDAS2 and Qualified Electronic Signatures (QES), passionate about advancing AI-driven legal technology? Do you have 8–20 hours per week to contribute alongside your current commitments? Join 10x Team and help shape how AI understands and applies digital identity and electronic signature standards in real-world scenarios.About the Role10x Team connects expert freelance professionals with leading AI labs to build next-generation solutions. We are seeking skilled consultants in e IDAS2 and Qualified Electronic Signatures (EU/UK) to enhance the quality, technical accuracy, and regulatory alignment of AI-driven systems.Key ResponsibilitiesReview and refine AI-generated content related to e IDAS2, QES, implementation guidelines, compliance scenarios, and practical best practicesAssess AI outputs for technical, legal, and regulatory accuracy and ensure alignment with current e IDAS2 standardsDevelop realistic scenarios illustrating digital identity, trust services, and signature workflows using your professional expertiseDraft scenario variations representing the perspectives of regulators, service providers, and end usersIdentify and correct gaps, inaccuracies, or faulty reasoning in AI-created materialApply your knowledge to ensure AI training data mirrors authentic regulatory analysis, processes, and documentationAbout YouSenior-level specialist with substantial professional experience in e IDAS2, Qualified Electronic Signatures, and digital trust frameworks in the EU or UKDeep understanding of compliance, standards, and real-world case applicationsSkilled in critiquing documents, compliance materials, and regulatory frameworksOrganized, detail-oriented, and able to provide actionable feedback independentlyAvailable 8–20 hours weekly and able to respond promptlyResidency in the UK or EU is requiredWhy Join 10x Team?Flexible, fully remote freelance work that fits your scheduleContribute directly to AI systems powering secure digital identity and trust solutionsFree access to our in-house AI Academy to deepen your AI expertiseStructured onboarding, clear project briefs, and ongoing collaborationHow to ApplyAfter applying, you’ll receive an email detailing the steps to:Complete a short written assessmentParticipate in an AI-powered interviewImportant: Your application is only complete once you finish all steps via the email link.Please note: these AI Lab missions are not traditional job openings with fixed start dates. Project demand is highly dynamic and matching depends on your expertise, availability, and current AI Lab needs. Some experts are matched within days, while others may wait longer for a suitable project.Help drive the future of AI-powered digital trust. Apply today and join 10x Team!#LI-TT1-----------------------------------------NOTEAt10x, there are two types of opportunities:1. Traditional freelance missionsThese are regular project-based opportunities where the listed mission is the actual project you may work on.2. AI Lab rolesFor AI Lab roles, we scout, review, and approve profiles for access to future project opportunities.The missions listed for AI Lab roles arenot traditional job openings. AI Lab work is often highly confidential as this exposes information of what an AI Lab is working on, and project requests are unpredictable. When an AI Lab request comes in, we often need to respond within24 hourswith suitable talent.Matching depends on the specific needs of each AI Lab project and your niche expertise. Once your profile is reviewed and approved, you may be matched to relevant AI Lab projects when suitable opportunities arise.This can happen within hours, but it may also take months, depending on the researchers at the AI labs and their project needs.

Experteer Overview In this role you will lead MRO u0026amp; Consumables sourcing across EMEA, aligning with regional regulatory standards and sustainability goals. You will drive cost optimization, supplier innovation, and ESG outcomes while leveraging digital procurement tools to generate measurable value. You’ll collaborate with plants, finance, and technical teams to shape category strategies and ensure supply assurance. This is a globally oriented, cross-functional role that offers impact across manufacturing sites and a chance to contribute to Bridgestone’s mission to serve society with superior quality. Compensaciones / Beneficios • Own end-to-end category strategies delivering cost savings, supply assurance, and value across EMEA sites • Lead suppliers and internal stakeholders to identify and implement cost reductions • Provide procurement support across functions and ensure procurement representation in business requirements • Analyze market trends and report issues and remediation plans to management • Develop sourcing strategies and drive implementation • Resolve quality, cost, delivery, and innovation issues • Foster a Continuous Improvement mindset (PDCA and Deming Plan) • Manage supplier performance through standardized processes and continuous improvement Responsabilidades • Strategic and/or Operational Procurement experience (5+ years) • Experience with direct/indirect goods and/or services in centralized, decentralized, or plant environments • Experience with MRO/Consumables category (Manufacturing Parts, Tooling, Process Aids, Chemicals, Rubber) • Experience with SAP and procurement digital tools (Fairmarket, Ariba, E-Catalogue) • Contract development, management, and oversight • Spend analysis, costing models, SWOT analysis, target costing, and clean sheet analysis • Tail spend management • Supplier risk assessment and mitigation strategies • Understanding of EU regulatory and GDPR and sustainability directives • Fluent in English Requisitos principales • Onboarding experience • Mentorship and development opportunities • Corporate social responsibility activities • Global, dynamic, challenging work environment • Work-life balance and well-being initiatives • Diversity and inclusion initiatives

CIDETEC in Spain is seeking a researcher for its Energy Materials Unit. Por favor, lea detenidamente la siguiente descripción del puesto para asegurarse de que encaja con el perfil antes de enviar su solicitud. This role involves working on lithium ion battery R&D, project management, and collaborating on European research initiatives. Ideal candidates will have a doctorate or master's in a relevant field, with over 3 years of experience in battery research and solid English skills. xcskxlj The company offers professional development opportunities and a supportive work environment. #J-18808-Ljbffr

ph3Company Description /h3 pTerry Soot Management Group (TSMG) is a field data collection company founded in 2017 in Europe. We collect data where automation is not possible. We count features, take pictures, make videos, record speech, and scan areas for every detail you need to make more informed decisions. Our field data collection teams are spread across Europe and North America, ready to accept new challenges. /p h3Project Overview /h3 pThis project aims to collect high‑quality visuals of streets, key points of interest, and public spaces across EU countries. Using vehicles equipped with removable 360° cameras and lidars, drivers will capture comprehensive images of the surroundings. The captured data will be stored on onboard computers (SSD Drives) and later utilized to enhance one of the world’s leading online mapping platforms. Data collectors will follow pre‑assigned routes, focusing on public streets, commercial areas, and points of interest. To ensure the highest image quality, certain areas may need to be revisited during favourable weather conditions. The duration of the project varies based on the scope of work required in each targeted data collection area. On average, the assignments involve 3 to 6 months of active work. /p h3Work schedule /h3 pFull time engagement within standard business hours (8 AM - 7 PM). /p h3Ideal Candidate /h3 ul liHolds a valid EU‑issued driver’s license /li liMaintains a clean background check (criminal and driving record) /li liHas at least 5 years of driving experience /li liPossesses professional driving experience (e.g., taxi, delivery, logistics) /li liProficient in English and the local language /li liTech‑savvy, with experience using GSuite tools (Gmail, Google Spreadsheets, Google Forms) /li liBasic knowledge of vehicle mechanics /li liDemonstrates responsibility, reliability, and professionalism /li liEnjoys traveling and exploring new places /li liFamiliar with the area of operations /li /ul h3What We Offer /h3 ul liA dynamic and engaging project that goes beyond just driving /li liCompetitive salary /li liComprehensive training covering both practical and theoretical aspects of data collection /li liOngoing support from experienced managers /li liThe opportunity to work in an international team and environment /li /ul /p #J-18808-Ljbffr

Insurance Compliance Counsel Antes de solicitar este puesto, por favor, lea la siguiente información sobre esta oportunidad que encontrará a continuación. Alan’s Insurance Compliance Counsel is the expert on members' insurance compliance and consumer protection regulation. The role defines how regulatory obligations translate into Alan's tools, processes, and products, owns the compliance posture on the perimeter, proactively manages exposure, and serves as the primary interface with regulators. What You Will Do • Define how regulatory obligations related to Alan’s core product (IDD, duty of advice, product governance, AML/CFT, etc.) translate into operational processes, product design, and tooling., • Suggest optimal ways to meet regulatory requirements within Alan's products while improving members' experience – from pricing components and options design to UX choices and complaint handling., • Proactively identify compliance risks, assess exposure, and develop mitigating action plans in coordination with internal stakeholders., • Lead the structuring and continuous improvement of Alan’s complaints management framework across France, Belgium, and Spain, ensuring compliance with ACPR recommendations and local equivalents., • Serve as the compliance function’s key contributor to Alan’s internal control system: document compliance‑related risks and controls in the Group’s centralised mapping, and co‑deploy the internal control approach across teams (Insurance, Operations, Sales, Care)., • Prepare and support internal and external audits: assess Alan’s standing against planned operational improvements, define remediation plans, and drive and monitor effective implementation., • Report on compliance obligations and risk exposure to Alan’s Board and governance committees, manage regulatory reporting obligations including the ACPR Questionnaire Protection de la Clientèle (QPC)., • Respond to regulatory inspections (ACPR, FSMA, or equivalent in Alan’s operating countries), coordinating internally and ensuring Alan is always audit‑ready., • Support the AML framework: conduct second‑level analysis on suspicious cases, manage relationships with regulatory bodies and financial intelligence units, approve high‑risk client relationships (including PEPs), and maintain the AML/CFT risk assessment framework., • Oversee KYC Ops referents’ training and upskilling, including Belgium‑specific AML requirements., • Coordinate with the AMLO on annual priorities, documentation, monitoring tools, and regulatory reporting to the ACPR and equivalent supervisors., • Maintain Alan’s compliance roadmap: prioritise, track progress, update the risk mapping, and re‑prioritise as the regulatory environment evolves., • Lead compliance projects with internal stakeholders across Insurance, Product, Sales, Care, and Operations, translating regulatory requirements into concrete deliverables and timelines., • Contribute to pragmatic compliance positions on regulatory requirements that affect our products and contracts – turning complex constraints into well‑reasoned, pragmatic solutions that support the business., • Design and maintain mandatory regulatory training programmes for Sales and Care roles (IDD competency requirements including duty of advice and product governance, Loi Evin, AML/CFT)., • Build internal compliance frameworks, guidelines, and decision‑making tools that increase team autonomy and reduce reliance on external resources., • Produce high‑quality documentation that teams can rely on independently., • Ensure Alan’s compliance standards travel consistently across all Group markets, adapting Group frameworks to local regulatory requirements and deploying them locally in coordination with local counsel. Experience & Skills • 4+ years of experience in compliance within an insurance or fintech company; solid coverage of at least two of the following: AML/CFT, insurance distribution (IDD), complaints handling, regulatory reporting., • Solid understanding of the French insurance regulatory framework and ability to work across EU/local requirements., • Proven ability to lead compliance projects cross‑functionally: translate regulatory requirements into clear priorities, align internal stakeholders, and deliver without creating bottlenecks or increased friction., • Bilingual French/English (both required, written and spoken)., • International exposure is a strong plus. You Will Thrive Here If You Are • A pragmatic problem‑solver who finds the right answer within regulatory constraints rather than defaulting to the most conservative one., • Rigorous and well‑organised, maintaining high documentation standards, tracking commitments, and keeping stakeholders informed., • Business‑minded, understanding what matters for the company’s growth and its members’ protection, and calibrating compliance work accordingly. Important Note We hire people, not roles. If you’re excited about this opportunity but don’t check every box, we’d love to hear from you. Everyone, no matter how underrepresented, should feel free to apply. If you identify yourself as a woman: research shows women often apply only when meeting 100% of requirements. Perks & Benefits • Alaners are provided with a stimulating environment and perks ensuring they are happy, efficient and spend only high‑quality time with co‑workers., • A strong culture – people joining Alan are often surprised and delighted by our innovative working method. xcskxlj We have a set of cultural values that guide our approach to work. #J-18808-Ljbffr

ppWork Travel Opportunity in Greece – Customer Support Agent /p pLocation : Greece (Athens or Work From Anywhere in Greece) /p pPosition : Customer Support Agent /p pLanguage : Spanish /p pWork Schedule : Monday – Friday | 10 : 00 – 01 : 00 (diverse shifts between these hours) /p pContract Type : Full-time /p pRemote Option : YES (WAH – Work At Home Available) /p h3Job Description /h3 pWe are looking for Spanish-speaking Customer Support Agents who want to combine an international work experience with the opportunity to live and work in Greece. This role is ideal for candidates seeking a Work Travel lifestyle while gaining valuable customer service experience in an international environment. /p h3Responsibilities /h3 ul liHandling inbound customer inquiries via phone, email, or chat /li liProviding professional and friendly customer support /li liResolving issues efficiently and accurately /li liEnsuring high customer satisfaction /li /ul h3Salary Benefits /h3 ul liSalary : €1,045 net / month /li liBonus : €200 monthly performance bonus /li liPaid training (10 days) /li liStable schedule (Monday–Friday) /li liWork-from-home option within Greece /li liRelocation Package /li li2 weeks hotel accommodation /li liFlight ticket (within the EU) /li liAirport pickup /li liReal estate agency fee covered /li liWAH Information: If relocating, WAH location is Athens. If already local, WAH is possible anywhere in Greece /li /ul h3Requirements /h3 ul liFluent Spanish (spoken written) /li liGood level of English /li liEU passport or valid EU work permit required /li liNo visa or work permit sponsorship provided /li liBasic computer skills /li liReliable internet connection /li liCustomer support experience is a plus /li /ul h3Important Notice /h3 pThis position does NOT offer visa or work permit sponsorship. /p pCandidates must already have the legal right to work in Greece / EU. /p h3Why Apply? /h3 ul liLive and work in beautiful Greece /li liPerfect Work Travel opportunity /li liCompetitive salary + performance bonus /li liRelocation support provided /li liInternational work environment /li /ul pApply now and start your Work Travel experience in Greece! /p /p #J-18808-Ljbffr

Alan is seeking an Insurance Compliance Counsel to translate regulatory obligations into actionable processes, product design, and tooling for a fintech/insurance company. ¿Quiere presentar una candidatura? Asegúrese de que su CV está actualizado y luego lea atentamente las siguientes especificaciones del puesto antes de solicitar. You will lead cross‑functional compliance projects, manage risk, and ensure audit readiness across multiple markets including Spain. The role requires strong knowledge of EU and local insurance rules, experience with ACPR/FSMA expectations, and fluent French and English. xcskxlj A pragmatic, business‑minded problem solver is preferred. #J-18808-Ljbffr

Nature of the Tasks Architecture and design of systems, under the domains of Cloud architecture, Application architecture, Infrastructure architecture or Data architecture. Review of the architecture of existing systems. Design and development of component architecture and building blocks. Analysis of requirements and modelling of Information Systems. Analysis of the integration possibilities of different information systems. Data analysis and data modelling. Coordination of the implementation of the technical architecture. Technical interfacing between the project leaders and the developers. Production of architecture documents. Participation in technical working groups, progress meetings and meetings with the users. Assistance in the analysis, testing, technical documentation, deployment, evaluation and reporting. Knowledge And Skills In-depth knowledge of the techniques and practices related to the relevant architectural domain (Cloud, application, infrastructure, data). In-depth knowledge of Service Oriented Architecture. In depth knowledge of applications design. In depth knowledge of modelling tools. Good knowledge of Enterprise Architecture. Good knowledge of Relational DBMS. Good knowledge of business process analysis. Knowledge of interoperability technology (e.G. web services, message oriented middleware, service oriented bus). Knowledge of software development methodologies (e.G. RUP, AGILE). Good redaction skills. Very good knowledge of GIT. Ability to give technical presentations. Ability to apply high quality standards. Ability to cope with fast changing technologies used in application architecture and design. Ability to participate in multi-lingual meetings, good communication skills. Capability of working in a team. Education And Experience Minimum 13 years of relevant studies and/or experience after the secondary school. Minimum 8 years of IT professional experience. Minimum 4 years of experience in architecture and design of information systems. Minimum 4 years of experience in development of information systems. Minimum 4 years of experience with UML, BPMN or equivalent Business Process Analysis or modelling tool. #J-18808-Ljbffr

Role: System Validation, Platform Qualification Location: Spain(100% Remote) Client: Infosys Sal: Market Range Permanent full-time position Requirements and number of open positions 3-5 years- 2 Positions in Open 5-10 Years- 2 Positions in Open 10+ years - 2 Positins in Open Role Overview We are looking for a highly experienced Validation resource with 10+ years of experience in Computerized System Validation (CSV) within the Life Sciences domain. The candidate will lead end-to-end validation activities for enterprise-level software systems and manage teams, stakeholders, and delivery for global programs. Key Responsibilities • Lead end-to-end validation lifecycle (Planning, Risk Assessment, Testing, Release, Periodic Review), • Drive validation strategy for enterprise programs across regions (Europe/Global), • Manage validation teams, allocate work, and ensure timely delivery, • Act as primary point of contact for client stakeholders and leadership, • Lead governance, status reporting, and escalation management, • Author and review validation deliverables (URS, FRS, IQ/OQ/PQ, RTM, Validation Report), • Ensure compliance with 21 CFR Part 11, EU Annex 11, Data Integrity (ALCOA+), • Manage quality processes (Deviation, CAPA, Change Control), • Support regulatory audits and inspection readiness, • Mentor and coach junior resources, build capability within the team, • Drive continuous improvement and standardization of validation processes Managerial Skills • Team leadership and people management, • Stakeholder and client relationship management, • Program and project management for global validation initiatives, • Risk and issue management with mitigation planning, • Resource planning and capacity management, • Governance, reporting, and executive communication, • Budget awareness and delivery management, • Cross-functional coordination across IT, QA, Business and Vendors Required Skills & Competencies • 10+ years of experience in Life Sciences CSV/CSA, • Exposure to cloud/SaaS validation, • Strong experience in enterprise systems (SAP S/4HANA, Veeva Vault, LIMS, QMS etc.), • understanding of SDLC and validation lifecycle, • Understanding on regulatory guidelines (GAMP 5, GxP, 21 CFR Part 11, EU Annex 11 etc.), • Experience in risk-based validation and CSA approach, • Experience working with US and European clients and regulated environments, • Strong documentation, communication, and leadership skills.