Trabajos compliance en BurgosCrear alertas

ph3Who are we: /h3 pAntolin is a leading global automotive supplier; we are experts in designing, manufacturing, and supplying innovative solutions for vehicles around the world. Our product portfolio includes trim, headliners, and cockpits, as well as lighting and other interior systems. We offer comprehensive solutions with a focus on quality, safety, and sustainability. Our products are used in many of the world’s leading car brands. In fact, Antolin equips nearly 700 vehicle models around the world. /p pWith 136 manufacturing plants and offices in 23 countries, Antolin has achieved this strong industry presence through 75 years of working with our customers in order to develop a complete cycle of component manufacturing, from their conception and design, through the development and validation stages, to their industrialisation and sequenced delivery. /p pWe are working hard on spearheading the transformation that the automotive industry is currently experiencing with regard to vehicle interiors by collaborating with our customers. We do so in order to develop more sustainable and technologically advanced vehicles that are also adapted to the new needs and requirements of their passengers. /p pAs part of this transformation, Antolin is committed to a sustainable business model that focuses on and creates value for all its stakeholders, including its customers, employees, investors, suppliers, and society as a whole. /p h3Mission: /h3 pProvide support to the Compliance and Data Protection Department in maintaining and strengthening the company’s compliance framework, assisting with operational, administrative, and monitoring activities related to regulatory compliance and data protection. /p h3Responsibilities: /h3 ul liSupport the management and updating of compliance and data protection policies, procedures, and documentation. /li liAssist in the preparation of internal training sessions and awareness materials. /li liCollaborate in the monitoring of actions and controls within the compliance system. /li liProvide administrative support in the handling of reports, queries, and incidents related to regulatory compliance. /li liAssist in document review and analysis related to data protection matters. /li liSupport the preparation of internal reports and presentations. /li /ul h3We are looking for: /h3 ul liDegree in Law (dual degree in Law Business Administration is a plus). /li liStrong interest in Compliance and Data Protection. /li liLanguages: Spanish, English /li liStrong organizational skills, attention to detail, and ability to work in a team environment. /li /ul h3What can we offer you: /h3 ul liYou will be part of a highly engaged multinational with international career opportunities. /li liWe offer you a learning journey adapted to your professional experience. /li liYou will work on international projects for world-renowned companies in Automotive sector. /li liYou can find an Open Environment to learn new technologies. /li liWe can offer you a competitive salary, benefits and valuable OEM discounts. /li /ul pHere at Antolin, we are an equal opportunity employer and value diversity in our workplace. We do not discriminate based on race, religion, colour, national origin, gender, sexual orientation, age, marital status, or disability status. All qualified applicants will receive consideration for employment without regard to any of these protected characteristics. We encourage applications from all individuals and strongly support diversity in our workplace. We strive to create an inclusive environment for everyone, and we are committed to treating everyone in a fair and equitable manner. We are proud to be an equal opportunity employer and are committed to fostering a diverse and inclusive work environment. /p pThis job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities. The Company reserves the right to revise the job description at any time. Duties, responsibilities or activities may change, or new ones may be assigned at any time with or without notice. The employee must be able to perform the essential functions of the position satisfactorily. If requested, reasonable accommodations may be made to enable employees with disabilities to perform the essential functions of the job, absent undue hardship. /p pDREAM. DARE. DO /p /p #J-18808-Ljbffr

Bussiness IT SpecialistApplylocations: Cojóbartime type: Full timeposted on: Posted Todayjob requisition id: VAC29255Reporting to our IT Director, you will ensure the planning, execution, and control of IT development projects to guarantee the fulfillment of the department’s project portfolio, following security standards.Job Description:Job Description:Site IT Accountabilities: Local IT Infrastructure tasks not in scope GITS (f.e. local asset management, phones, local contact for printer, switch, router maintenance/replacement on site, aid in remote user issues, document problem resolutions, assist GITS/NCC in software deployment, coordinate purchasing/receiving of new computer hardware and software as well as creating the Capex requests). Support in onboarding and off boarding of new employees. Assist in any required network diagnostic and upgrade(s) for the site(s). Ensures the data backup schedule is respected. Deployment of the Nutreco IT Policy. Deploy Risk Management according policy.Application Accountabilities: Provide application support and execute application maintenance for the local business applications, including but not limited to training, training materials, documentation of operating procedures and user manuals. Business applications include both common applications such as ERP and BU specific applications such as production software, labelling, LIMS, or other applications or systems. Create, co-ordinate and execute application testing towards user acceptance and in line with corporate requirements. Complete systems modifications, systems tests/audits on new and modified applications and assess system performance to ensure quality assurance as well as post implementation reviews. Collaborate and operationally manage external suppliers for support and maintenance of local business applications.Program project Management: Initiate new innovations and project proposals based on local requirements Manage local IT-related projects according to Nutreco standards and processes Responsible for local IT programIT Requirements Defines support requirements Transfers support requirements with Business IT Manager to Regional Service Manager or local suppliersEnvironment/IT Systems: Actively participates in the GITS / Unisys / Business IT triangle meetings. Travelling to the plants and other locations (if applicable) for any issues. Multi-task and manage multiple support calls meeting specific response times and deadlines. Participates in the development and execution of system implementation plans and solutions of the department. Work with technology teams and business unit as an in-house consultant and be prepared to lead or participate in broader initiatives panning all areas of Information System Adequate reporting and updating Business IT Manager.* Interaction with all levels of the business community as well as all levels of the IT organization.What you’ll bringWe’re looking for someone responsible and ready to take center stage in this role. Someone energetic, enthusiastic, eager to grow, and excited to collaborate with like‐minded people.You will also need: A degree in Systems Engineering, Computer Science, Industrial Engineering, or related fields. At least 3 years of experience in application development projects or application support. Basic knowledge of Agile and Waterfall project methodologies. Knowledge of the following technologies: + SQL + Reporting tools (PowerBI, Microstrategy, Qlik, Tableau, etc.) + At least one programming language (JavaScript, Java, .NET, Python, etc.) + No‐Code/Low‐Code tools (primarily PowerApps) + APIs Education: Bachelor’s or Master’s in Business, Computer Science or related field. Language: Fluent English; other languages are a plus.We also value knowledge in: Networks, switches, firewalls Microsoft operating systems Server maintenance Active DirectoryWhy You Will Love Working with Us:At Nutreco, you join a mission-driven organization committed to innovation, sustainability, and growth. You will have the opportunity to collaborate with leading minds across diverse disciplines while making a meaningful contribution to feeding a growing global population sustainably.We provide equal opportunities to all candidates. Applicants are considered for all roles without distinction of race, gender, religion, color, origin, age, status, sexual orientation, physical disability, or any other condition protected under applicable law.What we offer:Job Stability Based in BurgosCompetitive Compensation and Additional BenefitsContinuous Training and Professional GrowthAutonomy and ResponsibilityAs part of Nutreco, you will be a member of the SHV family, a diverse group of companies with a global presence. Join us and you’ll gain access to a broad network of expertise and international career paths. You will also benefit from the support of one of the largest privately owned companies in the world, known for its stability and long‐term vision.Our organisation:Skretting is a global leader in providing innovative and sustainable nutritional solutions and services for the aquaculture industry. Skretting has production facilities in 18 countries on five continents to manufacture and deliver high quality feeds from hatching to harvest for more than 60 species. The total annual production volume of feed is close to 2.5 million tonnes. Our mission is Feeding the Future.Equal Opportunity Employer:Skretting is an equal opportunity employer; applicants are considered for all roles without regard to race, color, religious creed, sex, national origin, citizenship status, age, physical or mental disability, sexual orientation, marital, parental, military status or any other status protected by applicable local law. Please advise us at any point during the recruitment and selection process if you require accommodation. Skretting is committed to compliance with all applicable legislation, including providing accommodation for applicants with disabilities.### About UsNutreco is a global leader in animal nutrition and aquafeed. Our advanced nutritional solutions are at the origin of food for millions of consumers worldwide. Its two global company brands Skretting(aqua feed) and Trouw Nutrition (animal nutrition) have sales in over 90 countries.Our purpose *Feeding the Future* captures a big challenge: feeding 9 billion people in 2050. Our responsibility is twofold: we need to make a significant contribution to meeting the rapid increase in worldwide demand for food; on the other hand, we need to find the right balance in order that we can realize growth while making also responsible choices for people and planet.To know more about us, please visit our website

pGSK in Burgos, Spain, seeks an experienced senior MSAT Drug Product lead to drive technology transfers, PPQ readiness, and lifecycle leadership for the drug product portfolio. You will coordinate cross‑functional teams, ensure robust control strategies, and support regulatory interactions to maintain product quality and compliance. /ppThe role requires strong technical leadership, hands‑on experience with solid dose manufacturing, and a proactive approach to continuous verification and process /p #J-18808-Ljbffr

ppINSUD PHARMA operates across the entire pharmaceutical value chain, providing specialized knowledge and experience in scientific research, development, manufacturing, sales, and marketing of a wide range of active pharmaceutical ingredients (API), finished dosage forms (FDF), and branded pharmaceutical products, adding value to human and animal health. /p pThe activities of INSUD PHARMA are organized into three synergistic business areas: Industrial (Chemo), Branded (Exeltis), and Biotech (mAbxience), with over 9,000 professionals in more than 50 countries, 20 state‑of‑the‑art facilities, 15 specialized RD centers, 12 commercial offices, and more than 35 pharmaceutical subsidiaries, serving 1,150 customers in 96 countries worldwide. INSUD PHARMA believes in innovation and sustainable development. /p pThe challenge: /p h3Specific Responsibilities /h3 ul liCollaborate with the Head of QA-RD in the implementation and maintenance of a Corporate Quality System in RD in compliance with GMP. /li liWrite and review corporate procedures which allow to standardize the RD Department activities and to assure their adaptation to the correspondent Good Manufacturing Practices. /li liReview and approve documents generated by RD (e.g. Analytical validations, master batch records, procedures, and analytical methods). /li liReview and approve executed batch records and analytical results of RD before their release. /li liIssue and review RD analytical specifications. /li liPerform internal and external audits. /li liCollaborate with the Head of QA-RD in the preparation and attendance of clients audits and Health Authorities inspections. /li liIssue and organize the documentation sent from QA to RA for new submission of MA and to answer DL. /li liCollaborate in GMP training of RD employees. /li liTrain the new incorporations in the specific activities and functions of the position in which you are an expert. /li /ul h3Requirements and personal skills /h3 ul liEducation: Degree in Health Sciences (e.g. Chemistry, Pharmacy, Biology or Medicine) with supplementary knowledge of Quality and GMP. /li liLanguages: Fluent Spanish and English, knowledge of other languages will be an asset. /li liExperience (years/area): +2 years in Quality Assurance and desirable experience in RD. /li liSpecific Knowledge: Quality procedures and GMP. /li liTravels: Not required, may occur occasionally. /li /ul h3COMMITMENT TO EQUAL OPPORTUNITIES /h3 pThe InsudPharma group is aware that business management must align with the needs and demands of society, and therefore assumes the commitment to equal opportunities and treatment between men and women, as stated in the current regulations on the matter - Organic Law 3/2007, and we do not discriminate against any person on the grounds of ethnicity, religion, age, sex, nationality, marital status, affective or sexual orientation, gender identity or expression, disability, or any other personal or social circumstance. /p pRD QA Technician Castilla and Leon, Spain /p /p #J-18808-Ljbffr

ph3Clinical Specialist Interventional - Spain /h3h3POSITION SUMMARY /h3pThe Spanish Clinical Medical Affairs (CMA) Specialist Interventional reports to the EMEA CMA Manager and is responsible for supporting the safe and effective use of the Interventional portfolio. The Clinical Specialist will assist with education programs and collaborate with key physicians health providers to provide country level education and clinical support. Working with the EMEA CMA Manager, the post will facilitate legal compliance with HCP interactions and education delivery. Clinical support and procedural education will be provided to physicians, nurses, technicians, etc. to include support for live cases/proctorships/scientific meetings and other educational programs in the therapeutic areas related to focus products. Society engagements facilitating the exchange of scientific information, in close collaboration with the CMA Manager and CMA Leadership team. The CS will assist the BU CMA Leader, BU Sales Leaders and Marketing department in the identification and delivery of appropriate internal and external customer training and education programs to support the Business Unit focused product portfolio. Excellent communication and interpersonal skills with the ability to trouble shoot medical device applications in a cardiology clinical setting are necessary. /ph3PRINCIPAL RESPONSIBILITIES /h3pAs an integral part of the CMA team, performance will be measured on delivery of assigned procedural education, its customer evaluations and feedback from the EMEA CMA leadership. /pulliSpecifically, a series of key metrics will be measured on a quarterly basis. /liliOverall completion of key strategic initiatives developed in conjunction with the EMEA CMA Leadership team. /liliCustomer support initiatives including education and training support and procedural support. /liliOverall EMEA CMA performance. /li /ulpKey responsibilities will include (but are not limited to) the following: /pulliClinical procedural training of customers in the use of the Teleflex Interventional portfolio to ensure safe and effective utilization of the product. /liliFacilitate the implementation of clinical workshops, live cases and proctoring for focused interventional products. /liliSupport pre-congress workshops and in-booth education programs. /liliDevelop and deliver educational activities ensuring compliance with Teleflex regulatory requirements. /liliCustomize, monitor and track product deployment plans for accounts in conjunction with the Manager. /liliMaintain training records and report these to CMA leadership. /liliSupport the educational grant process research submissions in conjunction with EMEA Clinical Manager and Global Scientific Research Services Team. /liliProvide clinical support to the commercial team and all customers. /liliAssist with the development and relationship maintenance of Key Opinion Leaders. /liliResponsible for clinical product training in conjunction with product manager (PM) and NSM for sales/marketing team members. /liliFacilitate training requests for approved education courses (on off site). /liliPerform field clinical trouble-shooting on the Company’s products by working with clinicians as required in collaboration with the QA/RA teams. /liliDevelop ethical, long-term customer relationships and represent the /liliCompany positively through field travel, clinical interaction, and medical/scientific meetings. /liliCollaborate communicate effectively across CMA, Marketing Sales team and remain compliant to Teleflex HCP policy and legal education requirements. /liliMaintain regular clinical credibility with Interventional cardiology and undertake /lilithe necessary revalidation requirements to maintain Registered Nurse status (if applicable). /liliOther assigned duties and responsibilities as required by CMA objectives. /li /ulh3EDUCATION / EXPERIENCE REQUIREMENTS /h3ulliQualification in the healthcare sector and registration with the relevant professional register. /liliDegree in medicine/clinical fields. /liliPossess a minimum of 2 years experience in Cardiology Interventional Nursing within a cardiac catheter laboratory. Alternatively, proven experience in the sector. /liliExperience in PCI and preferably with Chronic Total Occlusion (CTO) cases; experience in Structural procedures such as EVAR, TEVAR and TAVI procedures; experience in peripheral vascular interventions. /liliSkills and competencies in cardiac catheter laboratory and Vascular or Interventional Radiology nursing. /liliProven experience of education and teaching using simulation and workshop approaches. /liliExperience of developing and delivering teaching presentations to a group of health care professionals /li /ulh3SPECIALIZED SKILLS OTHER REQUIREMENTS /h3ulliExhibits strong written and verbal communication skills, as well as presentation skills. /liliExhibits strong time-management and organizational skills. /liliEstablished track record of building and maintaining relationships with internal and external customers. /liliProficient in Microsoft Office Suite. /liliSpanish native speaker and fluent English speaker. /liliClinical proficiency in area of clinical training. /liliDriving license. /liliPost will require frequent travel across Spain (up to 75%) and occasional and occasional trips abroad. /li /ulh3CULTURE: /h3pbCustomer Experience /b–Representing Teleflex in a customer facing position is a tremendous responsibility opportunity /ppAll CMA colleagues are expected to perform with the highest levels of professionalism, service, and ethics in order to strengthen the Teleflex brand and relationship with our customers. /ppbContinuous Improvement /b - Demonstrates initiative and critical thinking to identify and prioritize process and performance gaps. Develops solutions to deliver improving results. Exemplifies continuous improvement of thought processes and focus. /ppbCulture and Values /b – Exemplifies Teleflex values and ensures a fair, open, and productive climate that is engaging, ethical, and legally compliant. Strives to work effectively across boundaries in a complex matrix environment. Lead and participate in the process of promotional and other materials, working internally and cross-functionally to ensure materials are processed completely, based on accurate interpretation of clinical practice and data. /ph3TRAVEL REQUIRED /h3pUp to 75%. /ph3WORKING ENVIRONMENT /h3pTeleflex, Inc. is an affirmative action equal opportunity employer. D/V/M/F. Applicants will be considered without regard to age, race, creed, colour, national origin, ancestry, marital status, affectional or sexual orientation, gender identity or expression, disability, nationality, sex, or veteran status. If you require accommodation to apply for a position, please contact us at: . The description above represents the most significant duties of this role but is not all inclusive. Other work assignments comparable to the level of responsibility indicated above may be required. /p /p #J-18808-Ljbffr

At Bakelite, you’ll help us create a better tomorrow with sustainable and innovative chemistry today. We’re Everywhere. Everywhere you look, you’ll find products enabled by Bakelite, from stronger homes to safer automobiles and everywhere in between. With more than 100 years of history and strong customer relationships, we boldly engineer sustainable products to tackle our world’s most challenging demands.Experiencia, cualificaciones y habilidades interpersonales, ¿tiene todo lo necesario para triunfar en esta oportunidad? Descúbralo a continuación.Join Our Team and Help Us Build a Stronger, Safer, Better World. It’s Better with Bakelite.Europe Energy and Waste Engineer (all genders)What does a typical day look like? These are your main tasks: The Europe Energy and Waste Engineer supports EU Sites in identifying, developing and implementing energy efficiency, utilities optimization, and waste reduction initiatives, with the objective of reducing costs, ensuring regulatory compliance, and aligning with the company's sustainability strategy. The role conducts energy audits, identifies cost and GHG reduction opportunities, and provides technical guidance for sustainability programs. Through collaboration with operation teams ensures that practical solutions are implemented to improve environmental performance and reduce operating costs.Job ResponsibilitiesDevelop energy and utilities improvement programs, making sure implementation at site.Develop the EU Waste Reduction Program, aligning initiatives across sites and ensuring measurable reduction in disposal costs and environmental impact (zero waste initiatives).Collaborate with other Engineering Pillars to integrate energy‑efficient technologies, and waste reduction / elimination initiatives into capital projects and broader EU Engineering priorities.Conduct site audits to identify cost reduction and sustainability improvement opportunities. Rank opportunities and develop multi‑year site programs to implement projects and initiatives.Support ISO50001 implementation and EU sustainability goals.Develop and maintain energy and waste KPIs, providing regular reporting and benchmarking across sites.Facilitate workshops to generate improvement ideas.Collaborate with sites to implement metering systems and energy monitoring tools.Required Qualifications (Education & Experience)Engineering degree (energy, mechanical, environmental, electrical, or related discipline).Proven expertise in industrial energy and waste reduction and efficiency optimization.Proven track record of energy reduction and waste improvement.Strong facilitation and communication skills.Excellent English communication skills.Ability to work across multiple sites and cultures. xhfqzwm Equal Opportunity EmploymentWe are an Equal Opportunity, Affidative Action employer. All qualified applicants will receive consideration for employment without regard to gender, minority status, sexual orientation, gender identity, protected veteran status, status as a qualified individual with a disability or any characteristic protected by law.#J-18808-Ljbffr

A leading engineering company is seeking a Project Customer Support Engineer in Burgos, Spain. The role involves leading project execution, ensuring quality and timeline compliance, and maintaining client relationships. Ideal candidates will demonstrate strong negotiation skills, planning capability, and fluency in Spanish and English. This position offers opportunities to engage in diverse projects within an inclusive workplace environment.br#J-18808-Ljbffr

pBENTELER Group is seeking an OT Security Specialist to maintain and secure operational technology systems in industrial settings. You will bridge IT cyber security and production, coordinating across global and plant levels. /ppYou will contribute to policy development, collaboration with production areas, and the implementation of OT security governance, ensuring TCQ compliance and effective communication. /p #J-18808-Ljbffr

pAntolin, located in Burgos, Spain, is seeking a Compliance and Data Protection Support professional to aid in maintaining the compliance framework. Responsibilities include management of compliance policies, assisting in training sessions, and providing administrative support related to regulatory compliance. /ppThe ideal candidate will hold a Degree in Law, with a strong interest in compliance and data protection. Knowledge of Spanish and English is required. This position offers career growth opportunities in a multinational environment. /p #J-18808-Ljbffr

pCelebrity Cruises seeks an experienced bakery professional to join our shipboard team, delivering high-quality bread production, presentation, and display across daily menus while upholding the ship’s standards and guest expectations. /ppResponsibilities include assisting the Head Baker with forecasts, managing leftovers to control costs, ensuring USPH compliance, supervising cleanliness, coordinating with others, and attending training sessions as required. /p #J-18808-Ljbffr

pCelebrity Cruises seeks an experienced Baker to manage daily bakery operations aboard the ship, ensuring high quality bread for all menus. You will support forecasts, monitor leftovers, and keep waste and food costs within budget while maintaining USPH compliance. /ppYou will assist in display setups and daily cleaning, train team members, and participate in shipboard meetings and training as required. /p #J-18808-Ljbffr

Position Summary You will manage the Manufacturing Science and Technology (MSAT) Drug Product technical delivery for drug product manufacturing of a defined product or product family with a primary focus on New Product Introduction (NPI) and successful product launches, including delivering successful right-first-time product qualifications. You will work with cross‑functional teams across functions to ensure robust product control strategies are implemented at manufacturing sites. We value clear problem solving, practical scientific judgement, and collaborative leadership. This role offers growth, meaningful impact and the chance to help GSK unite science, technology and talent to get ahead of disease together. Responsibilities Act as the single technical point of contact for the drug product portfolio, owning technical risk, decision‑making and product knowledge. Lead and deliver technology transfers to internal sites and external manufacturers, including transfer packages, training and readiness reviews. Manage continued process verification, process performance qualification and change management to maintain product robustness and compliance. Drive right‑first‑time execution of product qualification activities (e.G., PPQ/qualification readiness), managing appropriate governance through the relevant stage‑gate forums as the program approaches PPQ, ensuring robust data, clear acceptance criteria and effective issue resolution. Define and maintain product control strategy and technical risk assessments. Translate that knowledge into clear documentation for operations. Support regulatory submissions and post‑approval inspections by providing technical input, comparability strategies and supporting documentation. Manage cross‑functional investigations, root cause analysis and corrective actions for complex deviations and quality events. Basic Qualifications Bachelor’s degree in a relevant scientific, engineering or technical discipline. Minimum 10 years’ experience in pharmaceutical development, manufacturing or MSAT roles. Demonstrated experience in technology transfer, process validation and product lifecycle technical leadership. Practical knowledge of Good Manufacturing Practice (GMP) and regulatory expectations for drug product manufacture. Experience applying risk assessment approaches, process control strategies and quality tools to maintain product performance. Familiarity with regulatory dossiers and supporting health authority questions. Strong written and verbal communication skills and experience working with multi‑disciplinary teams. Hands‑on experience with oral solid dose drug product manufacturing. Preferred Qualifications Advanced degree (MSc, Ph D) in a relevant scientific or engineering discipline. Experience with Quality by Design, continued process verification and statistical process control. Track record of leading complex technical investigations and delivering sustainable corrective actions. Experience supporting regulatory filings, inspections and readiness activities. Ability to lead improvement projects that demonstrate measurable technical or operational value. US annual base salary for new hires in this position ranges from $125,250 to $208,750. GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law. #LI-GSK #J-18808-Ljbffr

ppbPosition: /b QA Specialist (PRD) – Investigations, CRs, CAPAs Floor Oversight /p pbLocation: /b León (on-site) /p pbExperience: /b At least 3 years’ experience in similar roles within the Quality department in pharmaceutical industrial settings /p pWe are looking for a QA Specialist (PRD) – Investigations, CRs, CAPAs Floor Oversight who is passionate about the industrialisation of new products. /p h3General Responsibility /h3 pEnsure quality oversight of production-related activities in a GMP-regulated manufacturing environment, acting as a key quality partner for operations on the shop floor. The role is responsible for leading and coordinating investigations, change controls and CAPAs, ensuring appropriate risk assessment, impact evaluation and timely closure in compliance with quality and regulatory requirements. In addition, the position provides real‑time QA support to production, reinforcing GMP compliance, issue resolution and continuous improvement across daily manufacturing operations. /p h3Specific Responsibilities /h3 ul liLead and manage quality investigations related to deviations associated with production activities. /li liPerform and support root cause analysis, ensuring robust identification of underlying causes and appropriate documentation of findings. /li liEvaluate the impact of deviations on product quality, manufacturing processes and GMP/regulatory compliance. /li liCoordinate cross‑functional investigation activities with Production, Engineering, Quality Control, Maintenance and other relevant departments. /li liReview, assess and approve change requests/change controls, ensuring proper justification, impact assessment and implementation in line with GMP requirements. /li liEnsure that change controls are adequately evaluated, approved, implemented and closed within established timelines. /li liReview and approve CAPA plans derived from investigations, audits and inspections, ensuring actions are appropriate and sustainable. /li liMonitor CAPA implementation and verify effectiveness prior to closure. /li liProvide routine QA floor oversight through regular presence in production areas, supporting real‑time decision‑making and compliance with approved procedures. /li liSupport production teams during critical operations, helping resolve GMP issues promptly and reinforcing quality culture on the shop floor. /li /ul h3Experience (area) /h3 pQuality Assurance in GMP‑regulated pharmaceutical or biotechnology manufacturing environments, with strong exposure to production‑related quality activities. /p h3Personal Skills /h3 ul liAdaptability to change and flexibility /li liSpeed without compromising on quality /li liLeadership and teamwork /li liEffective communication /li liCompliance, integrity and sustainability /liliGrowth mindset /li liBusiness focus /li /ul h3Our Benefits /h3 ul liPermanent contract /li liCareer progression and development within a growing international group /li liOngoing training and an innovative working environment /li liSubsidised canteen and other employee benefits /li /ul pCOMMITMENT TO EQUAL OPPORTUNITIES AT LEONFARMA, we believe in and act to promote genuine equality of opportunity. We do not discriminate on the basis of gender, ethnicity, religion, sexual orientation, disability or any other characteristic. We value diversity and talent. We’d love to meet you! /p /p #J-18808-Ljbffr

ph3Overview /h3 pIn this role, you will lead MSAT Drug Product delivery with a focus on new product introductions and successful launches. You’ll act as the technical lead for the drug product portfolio, coordinating technology transfers across sites and ensuring robust control strategies. You will work with cross‑functional teams to maintain product robustness, support regulatory interactions, and drive right‑first‑time qualification and continuous verification. You’ll help scale science and technology to get ahead of disease while leading critical technical investigations and improvements. /p h3Responsibilities /h3 ul liBe the single technical point of contact for the drug product portfolio, owning technical risk and product knowledge. /li liLead and deliver technology transfers to internal sites and external manufacturers, including transfer packages and readiness reviews. /li liManage continued process verification, process performance qualification and change management to keep product robustness and compliance. /li liDrive right‑first‑time execution of product qualification activities (PPQ readiness) with strong governance and clear acceptance criteria. /li liDefine and maintain product control strategy and risk assessments, translating knowledge into clear documentation for operations. /li liSupport regulatory submissions and post‑approval inspections with technical input and comparability strategies. /li liCoordinate cross‑functional investigations, root cause analysis and corrective actions for deviations and quality events. /li /ul h3Qualifications /h3 ul liBachelor’s degree in a relevant scientific, engineering or technical discipline. /li li≥8 years’ experience in pharmaceutical development, manufacturing or MSAT roles. /li liExperience in technology transfer, process validation and product lifecycle technical leadership. /li liPractical knowledge of GMP and regulatory expectations for drug product manufacture. /li liExperience applying risk assessment approaches, process control strategies and quality tools. /li liFamiliarity with regulatory dossiers and health authority questions. /li liStrong written and verbal communication skills with multi‑disciplinary teams. /li liHands‑on experience with oral solid dose drug product manufacturing. /li /ul h3Benefits /h3 ul liAnnual bonus. /li liLong‑term incentive program. /li liHealth care and other insurance benefits. /li liRetirement benefits. /li liPaid holidays, vacation and leave. /li /ul pLocation: Burgos, Kingdom of Spain /p /p #J-18808-Ljbffr

Experteer Overview In this role, you will lead MSAT Drug Product delivery with a focus on new product introductions and successful launches. You’ll act as the technical lead for the drug product portfolio, coordinating technology transfers across sites and ensuring robust control strategies. You will work with cross-functional teams to maintain product robustness, support regulatory interactions, and drive right-first-time qualification and continuous verification. You’ll help scale science and technology to get ahead of disease while leading critical technical investigations and improvements. Compensaciones / Beneficios • Be the single technical point of contact for the drug product portfolio, owning technical risk and product knowledge • Lead and deliver technology transfers to internal sites and external manufacturers, including transfer packages and readiness reviews • Manage continued process verification, process performance qualification and change management to keep product robustness and compliance • Drive right-first-time execution of product qualification activities (PPQ readiness) with strong governance and clear acceptance criteria • Define and maintain product control strategy and risk assessments, translating knowledge into clear documentation for operations • Support regulatory submissions and post-approval inspections with technical input and comparability strategies • Coordinate cross-functional investigations, root cause analysis and corrective actions for deviations and quality events Responsabilidades • Bachelor’s degree in a relevant scientific, engineering or technical discipline • ≥8 years’ experience in pharmaceutical development, manufacturing or MSAT roles • Experience in technology transfer, process validation and product lifecycle technical leadership • Practical knowledge of GMP and regulatory expectations for drug product manufacture • Experience applying risk assessment approaches, process control strategies and quality tools • Familiarity with regulatory dossiers and health authority questions • Strong written and verbal communication skills with multi-disciplinary teams • Hands-on experience with oral solid dose drug product manufacturing Requisitos principales • annual bonus • long term incentive program • health care and other insurance benefits • retirement benefits • paid holidays • vacation and leave

pTeleflex is seeking a Clinical Specialist Interventional to support education and clinical use of the Interventional portfolio across Spain. The role involves working with physicians, nurses, and technicians to deliver education, live cases, and proctoring, while ensuring compliance with regulatory requirements. /ppThe ideal candidate will have nursing or medical qualifications, at least two years in cardiology interventional settings, and experience in PCI/CTO and related procedures. /p #J-18808-Ljbffr

ABB in Spain is looking for a skilled technician to execute automation projects, offering services such as commissioning and maintenance. The role includes working with the team and clients to ensure high-quality solutions in compliance with industry standards.This hybrid role allows remote work for candidates throughout Spain while favouring those in Burgos or nearby. Ideal candidates will possess a degree in Electronics, Robotics, or Automation and have solid experience in PLC programming and technical assistance.

UMAFLEX INDUSTRIA DE MOVEIS COLCHOES E ESPUMAS LTDA está em busca de um responsável ambiental para acompanhar e garantir o cumprimento das normas ambientais na empresa, promovendo a sustentabilidade.As responsabilidades incluem inspeções ambientais diárias, elaboração de relatórios e gerenci

pBanco Santander in Burgos seeks a Private Banking Banker to manage a portfolio of affluent clients with personalized investment guidance. /ppYou will build long-term relationships, advise on wealth solutions, and collaborate with a dynamic team to drive client satisfaction and growth in Private Banking across the region. /ppFluency in Spanish and English supports diverse client communications and regulatory compliance in the local market. /p #J-18808-Ljbffr

The successful applicant will ensure compliance with safety and quality regulations while leading project teams to achieve project success.

Talent is looking for a Solution Designer to support their strategic growth initiatives in accounting and compliance across Europe.

MSD Malaysia is seeking a tax professional to join its Spain-based Tax team, contributing to transfer pricing, tax compliance, and audits.

Una empresa farmacéutica innovadora busca un analista fisicoquímico para realizar análisis de productos inyectables.En esta emocionante posición, serás responsable de llevar a cabo análisis de materias primas y productos finales, así como de gestionar materiales de laboratorio y contribuir a

Dormont Manufacturing Co, ubicada en León, España, busca un Responsable de Garantía de Calidad para asegurar el cumplimiento de las normativas GMP mediante la gestión y mejora de los sistemas de calidad.Esta posición ofrece modalidad híbrida con un día de teletrabajo a la semana.Los candidato

PCI Pharma Services busca un/a QA Specialist (Validaciones) para garantizar el cumplimiento de GMP y la liberación de productos seguros y de alta calidad.Colaborarás con Producción, Ingeniería, Control de Calidad, I+D y Registros, participando en cualificaciones, validaciones y mejoras continuas

A global HR service provider based in Spain is seeking detail-driven professionals for a project-based role focused on supporting HR compliance initiatives.

A biotechnology company in Spain is seeking a candidate for an operations support role.The position involves applying for research funding, managing patents, and drafting contracts.Candidates must have a degree in life sciences, ideally in biotechnology or biomedical engineering, and proficiency in

You will oversee complaints, CAPAs, returns, recalls, and site service compliance with internal procedures, GMPs, authorities and customer requirements.

People Corporation seeks a Welfare Administrator to manage member benefit entitlements under a collective bargaining framework.You will verify employer contribution reports, balance and audit complex datasets, and ensure accurate benefit calculations while coordinating with union representatives and

Contribute to compliance processes and minimum standards by identifying opportunities to improve adherence to quality standards, procedures, and company standards. An interest in compliance and a willingness to deepen your knowledge. Our Compliance team blends regulatory expertise with data‑driven

We are expanding rapidly and seek an experienced Senior Tax Compliance Consultant (pan-European VAT) to lead high-quality services and mentor the team.

Revolut is seeking a Financial Crime Compliance Manager to strengthen quality control and risk management in a fast‑moving digital environment. You will contribute to high‑standard compliance processes while supporting safe, scalable product.

Govern Allianz Risk Shield (ARS) programme execution across CTO2 environments, including planning, tracking and reporting of compliance progress: monitor self‑attestation, evidence collection, testing progress, control effectiveness and compliance‑score targets, drive remediation and uplift acti

Coordinate selected compliance topics and contribute to the development of a group-wide compliance framework. Initial experience in compliance, governance or risk management is a plus. Tech_Data Protection & Compliance Specialist for BeTerna.

We’re looking for a Head of Regulatory Compliance who will lead regulatory compliance efforts in Revolut Bank UAB branches. Working with Regulatory Compliance Managers to ensure that local compliance management frameworks and processes are aligned with global ones. Building and leading a team of r

Oxigent Technologies busca un/a Responsable de Gobierno del Dato para liderar un proyecto estratégico en Palma de Mallorca, definiendo e implantando un modelo corporativo de Data Governance y asegurando la calidad, seguridad y trazabilidad de la información.Data Governance, con liderazgo transvers

Coordinating and animating the local network of Ethics & Compliance Representatives. Professional experience as a lawyer or compliance manager in an international environment a plus. A position of Temp Spain - Compliance Manager has just opened within Airbus in Madrid, Spain.

You will own the in‑country employment lifecycle, ensure payroll, compliance, and HR operations are executed flawlessly, and resolve complex client issues with stakeholders across legal, payroll, onboarding, and finance.

You will liaise with local payment schemes, ensure regulatory compliance, and oversee end-to-end payment operations and issue resolution with partners. You will collaborate with IT and compliance teams while staying ahead of regulatory changes and market trends to continuously strengthen Revolut's p

BeOne Medicines is seeking a Regional Clinical Compliance Country Manager for Spain to oversee country and site-level GCP compliance and risk management.

Regional Clinical Compliance Country Manager is responsible for ensuring robust oversight of clinical trial compliance at the country and site level. This role applies a risk-based approach to proactively identify, evaluate, and manage compliance risks, ensuring adherence to Good Clinical Practice (

Approximately 10-15 years of relevant consulting or industry experience in EHS compliance, environmental permitting, due diligence, auditing, or risk management. Interest in developing expertise in transaction advisory, EHS compliance, and risk management. EHS Due Diligence & Compliance Manager.

Revolut is seeking a Regulatory Compliance Manager to ensure consumer protection and regulatory requirements across the EEA. You will advise the business on compliance controls, shape policies from scratch, and oversee training programs while ensuring marketing communications meet regulatory standar