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Role: Configuration Expert – SC Demand & Distribution PlanningRecuerde revisar su CV antes de enviar la solicitud. Además, asegúrese de leer todos los requisitos relacionados con este puesto.Location: Barcelona / Meridian OfficeType of work: Hybrid / Full timeSanofi Supply Chain TransformationOver the last several years, Sanofi has embarked on a transformation program of Digital Supply Chain processes, and related information systems, including distribution, customer service, and planning systems.Under the main transformation program SCCORE, a major stream is Supply Chain Planning, which includes the implementation of the Kinaxis planning system covering forecasting and demand planning, S&OP/IBP, Distribution Resource Planning (DRP), multi-sites planning (MSP), and CMO collaboration, as a Core Model. The Kinaxis Core Model is being Progressively implemented worldwide for each Global Business Unit.SCCORE has evolved to support the ambitions of the recently launched Smart Supply Chain program which has a main objective to implement a smart supply chain from supplier to patient. SCCORE and Smart Supply Chain are taking place in parallel with, and in support of, other company strategic programs such as iSHIFT program (integrated ERP for Manufacturing, Distribution and Finance).These transformation programs are aligned with an agile transformation and the evolution of our ways of working to become more flexible, adaptable, collaborative, and user‑centric.Main ResponsibilitiesYou will configure and maintain Kinaxis Maestro (formerly RapidResponse) solutions that enable Sanofi to effectively plan demand and support IBP and S&OP processes across global markets and business units. You will ensure that demand planning processes, forecasting models, demand reviews, and cross‑functional planning workflows are supported by accurate, reliable, and scalable configurations.You will collaborate with Product Owners, demand planners, commercial teams, finance partners, and supply chain stakeholders to translate business requirements into system configurations, ensuring end‑to‑end visibility and alignment between market demand, business objectives, and operational plans.Other Specific Responsibilities IncludedConfigure and customize Kinaxis Maestro modules for Demand Planning, Forecasting and IBP‑PBF set ups.Support integration of downstream data flows, including part customers, forecast items, management centers, sales/actuals, valorization (COGS), and segmentation data.Analyze the impact of Kinaxis releases on downstream planning solutions and propose remediation or configuration updatesDesign and support implementation on Kinaxis integration model with multiple SAP ERP systems globally, ensuring data flow is seamless and efficientCollaborate with stakeholders across within SC organization (including Statistical Forecasting, Analytics and SC Digital Intelligence), Finance, Markets, DCs and third‑party customers to capture requirements and design effective configurationsMaintain and improve existing downstream configurations to optimize supply‑demand balance and Sanofi SC infrastructure / networkTroubleshoot and resolve downstream planning configuration issues, ensuring minimal disruption to S&OP monthly cycleDocument configurations and solutions in JIRA, Confluence, and other xhfqzwm repositories to ensure knowledge sharing and traceabilityParticipate in Agile ceremonies and contribute to iterative delivery of downstream planning solutions by performing System Integration Test (SIT) as well as collaborating on the training materials and User Acceptance Test (UAT)Ensure compliance with Sanofi’s governance, security, and quality standards, including GxP where relevantAbout YouMinimum 3 years of experience in supply chain systems configurationBachelor’s degree in Computer Science, Information Systems, Engineering, Supply Chain, or related fieldKinaxis configuration experience, with focus on demand planning is a plusFluent in EnglishStrong analytical, problem‑solving, and communication skillsPrior experience in the pharma/chemistry industry with knowledge of Supply Chain management is plusIT environments experience or SAP and Kinaxis knowledge is also plusExperience with Agile methodologies and usage of JIRA and Confluence#J-18808-Ljbffr

Material Scientist Applylocations: Barcelona: Baie-D'Urfé: Boston: London: Uppsalatime type: Full timeposted on: Posted Todayjob requisition id: JR018321 Galderma is the emerging pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services that span the full spectrum of the fast-growing dermatology market through Injectable Aesthetics, Dermatological Skincare and Therapeutic Dermatology. Since our foundation in 1981, we have dedicated our focus and passion to the human body's largest organ - the skin - meeting individual consumer and patient needs with superior outcomes in partnership with healthcare professionals. Because we understand that the skin, we are in shapes our lives, we are advancing dermatology for every skin story. We look for people who focus on getting results, embrace learning and bring a positive energy. They must combine initiative with a sense of teamwork and collaboration. Above all, they must be passionate about doing something meaningful for consumers, patients, and the healthcare professionals we serve every day. We aim to empower each employee and promote their personal growth while ensuring business needs are met now and into the future. Across our company, we embrace diversity and respect the dignity, privacy, and personal rights of every employee. At Galderma, we actively give our teams reasons to believe in our bold ambition to become the leading dermatology company in the world. With us, you have the ultimate opportunity to gain new and challenging work experiences and create an unparalleled, direct impact. Further supporting our growth and innovation momentum, we are establishing a new Global Capability Center in Barcelona to deploy new capabilities to effectively support its global commercial and functional teams. Located in the upscale Eixample District in the heart of Barcelona, Galderma’s Global Capability Center offers numerous possibilities for professional development such as exposure to global and cross-functional projects and access to global career opportunities.Job Title: Material Scientist Location: Barcelona, Spain ; Baie-D'Urfé, Canada; Uppsala, Sweden; Boston, US; London, UK. At Galderma, we’re looking for a hands-on Material Scientist to join a small, highly technical team where expertise, curiosity, and critical thinking truly matter. This role is ideal for someone who doesn’t just study materials—but understands how they interact, behave, and impact real products in a regulated environment.Your ImpactYou will bring deep technical expertise to understand, characterize, and optimize materials, ensuring performance, compatibility, and scalability across our products and packaging systems.What You’ll Do Analyze and characterize materials and their chemical composition and behavior Understand interactions between raw materials and packaging (tubes, bottles, etc.) Assess how supplier differences impact material performance and product quality Investigate material-related issues and drive practical, science-based solutions Collaborate closely with cross-functional teams across Product Science, MS&T, and Quality Translate complex findings into clear technical documentation and presentationsWhat You Bring MSc or Ph D in Material Science, Chemistry, or related field 3–8+ years in pharma, biotech, cosmetics, or injectable/aesthetic products Strong expertise in material characterization and analytical techniques Deep understanding of material interactions and applied science (not theoretical-only) Hands-on mindset with strong problem-solving and critical-thinking skills Excellent technical writing and presentation abilities* applied material science in regulated industries (e.G., pharma, aesthetics, cosmetics)Our people make a differenceAt Galderma, you'll work with people who are like you. And people that are different. We value what every member of our team brings. Professionalism, collaboration, and a friendly, supportive ethos is the perfect environment for people to thrive and excel in what they do.#J-18808-Ljbffr

Tu nueva empresa Compañía del sector farmacéutico con un fuerte enfoque en calidad, cumplimiento GMP y desarrollo de nuevos proyectos para clientes internacionales, que requiere de la incorporación de un/a técnico/a a HSE/ PRL. Tu nuevo puesto Garantizar la implantación, seguimiento y mejora continua de los sitemas de HSE en planta química-farmacéutica, asegurando el cumplimiento de la legislación, políticas corporativas y los estándares de seguridad de proceso. Entre tus principales funciones : Liderar y participar en análisis de riesgos de proceso (HAZOP, What If, FMEA, LOPA, Bow Tie). Evaluar modificaciones de instalaciones mediante procedimientos de Management of Change (MOC). Colaborar en la definición de medidas de protección frente a riesgos ATEX, incendios y explosiones. Garantizar la correcta gestión de sustancias peligrosas, inflamables, tóxicas y corrosivas. Participar en estudios de seguridad y cumplimiento de normativa Seveso cuando aplique. Desarrollar, implantar y supervisar el Plan de PRL. Realizar evaluaciones de riesgos en áreas productivas, laboratorios, almacenes y servicios auxiliares. Investigar accidentes, incidentes y casi accidentes, definiendo acciones correctivas y preventivas. Coordinar actividades empresariales (CAE) con contratistas y empresas externas. Impartir formación e información en materia de PRL a empleados y colaboradores. Participar activamente en auditorías internas y externas. Qué necesitarás para encajar con el puesto Grado universitario en Ingeniería Química, Química, Ciencias Ambientales, Farmacia, otras titulaciones afines. Máster en PRL con las tres especialidades (Seguridad en el Trabajo, Higiene Industrial y Ergonomía y Psicosocilogía aplicada). Qué obtendrás a cambio Incorporación a una empresa consolidada y en crecimiento dentro del sector farmacéutico. Participación en proyectos innovadores con clientes internacionales. Desarrollo profesional en un entorno altamente especializado en calidad. Horario flexible de lunes a viernes. Tu siguiente paso Si estás interesado en esta oferta, haz click en "aplicar ahora" para enviar una copia actualizada de tu CV, o llámanos ahora.

A leading AI healthtech company in Barcelona is seeking a Director of Business Development / Clinical Solutions for Europe. This pivotal role involves driving the sales cycle and nurturing relationships with biopharma partners. Candidates should have over 5 years of experience in business development within biotech or pharma, a strong understanding of clinical trials, and the ability to close enterprise deals. The company offers competitive pay, health benefits, and a flexible hybrid work model.#J-18808-Ljbffr

Compañía internacional especializada en servicios farmacéuticos, distribución regulada y soporte a ensayos clínicos ¿Es este el siguiente paso en su carrera? Descubra si es el candidato adecuado leyendo la descripción completa a continuación. ¿Buscas un proyecto con impacto real y recorrido hacia Dirección de Operaciones? Estamos creando una posición estratégica dentro de una compañía farmacéutica internacional en plena fase de crecimiento. Buscamos una persona con experiencia en operaciones farmacéuticas que quiera asumir un rol transversal, participando en la coordinación diaria del negocio y contribuyendo activamente a la evolución de los procesos, sistemas y estructura operativa de la organización. Esta posición está concebida como un paso natural hacia una futura responsabilidad como COO Deputy, trabajando muy cerca de la Dirección de Operaciones y Dirección General. ¿Cuál será tu misión? Serás el punto de conexión entre clientes, operaciones y departamentos internos, garantizando que los procesos se ejecuten de forma eficiente, escalable y alineada con los estándares de calidad y compliance del sector farmacéutico. Participarás en la gestión y mejora de operaciones relacionadas con: • Distribución farmacéutica regulada., • Gestión de pedidos y seguimiento operativo., • Documentación crítica y trazabilidad., • Coordinación con Quality y Regulatory., • Gestión de incidencias y escalaciones., • Reporting operativo y KPIs., • SOPs, mejora continua y optimización de procesos., • Automatización y uso de herramientas digitales e IA. Nos interesan especialmente profesionales procedentes de entornos como: • Distribución farmacéutica bajo GDP/BPD., • CROs y Sponsors. Experiencia en entornos farmacéuticos regulados. Conocimiento de procesos GDP/BPD. Capacidad para crear SOPs, KPIs y procesos escalables. Mentalidad analítica y orientación a la mejora continua. Nivel alto de inglés (B2+/C1). Interés por la automatización, reporting y herramientas digitales. Posición de nueva creación con alto impacto en la organización. Participación directa en proyectos estratégicos de crecimiento. Exposición transversal a todas las áreas del negocio. Entorno internacional y altamente regulado. Desarrollo profesional con recorrido hacia COO Deputy. Formación y acompañamiento en el negocio. Teletrabajo 1 día por semana tras periodo de formación. Horario: Lunes a jueves: 8:30 a 17:45h // Viernes: 8:30 a 14:30h Salario incluyendo variable, según valia 35-40k ¿Por qué puede ser diferente a otras posiciones? Porque no buscamos una persona para gestionar pedidos. xcskxlj Buscamos a alguien que quiera entender la operación de principio a fin, impulsar mejoras, conectar áreas clave del negocio y evolucionar hacia una posición de liderazgo dentro de una compañía farmacéutica internacional. #J-18808-Ljbffr

S&you España busca un perfil con experiencia en operaciones farmacéuticas para coordinar el día a día del negocio y evolucionar procesos, sistemas y estructura operativa de la organización. Si está considerando enviar una solicitud, asegúrese de pulsar el botón de solicitar de abajo después de leer la descripción completa. La posición es estratégica, con posible recorrido hacia COO Deputy, exposición transversal y entorno internacional regulado; teletrabajo xcskxlj 1 día/semana tras formación, con salario 35-40k y foco en automatización y KPIs. #J-18808-Ljbffr

Compañía del sector farmacéutico con un fuerte enfoque en calidad, cumplimiento GMP y desarrollo de nuevos proyectos para clientes internacionales, que requiere de la incorporación de un/a técnico/a a HSE/ PRL.Garantizar la implantación, seguimiento y mejora continua de los sitemas de HSE en p

Melt Group está buscando un/a Pharma Operations Specialist para unirse a su equipo en Sant Adrià de Besòs, España.

APM Terminals At APM Terminals, a global leader in port and terminal operations, we enable global trade and drive sustainable growth. What drives us forward is a mindset of always improving — observing how work happens, identifying what creates value, and removing what gets in the way. We constantly look for smarter, simpler, and safer ways of operating. If you thrive in environments where people value learning and are committed to continuously improve daily operations, join us and be apart of our journey.What We Can Offer:Foster a dynamic learning and training culture that empowers our employees to excel.Our commitment to improvement is driven by Lean principles, ensuring that every team member has the opportunity to develop their skills and advance their careers.Experience a diverse, multinational workplace where your operational insights directly influence how we work.Work in a global, matrix organisation with exposure to senior leadership and international stakeholders.Opportunities to shape finance strategy and influence terminal performance.Ongoing development through on-the-job learning, leadership exposure, and strategic projects.Collaborative environment focused on continuous improvement and operational excellence.Role OverviewWe are APM Terminals, and we are looking for a Chief Financial Officer (CFO) to lead the finance function across the cluster of Spain Gateways, including Valencia, Gijón, and Barcelona, as well as other related legal entities. You will act as a strategic business partner to the Managing Director, driving financial performance, governance, and long‑term value creation. This role combines financial leadership with operational insight, enabling data‑driven decisions across the business.Key ResponsibilitiesLead the finance function, covering accounting, planning, performance management, governance, risk, and compliance.Ensure accurate and timely financial reporting across processes including Record‑to‑Report, Order‑to‑Cash, and Procure‑to‑Pay.Drive financial planning, analysis, and investment evaluations to support strategic and operational decisions.Establish and maintain robust internal control, risk management, tax, and compliance frameworks.Partner with the Managing Director and leadership team to execute business strategy and improve financial outcomes.Lead finance transformation initiatives (e.G., system changes, process improvements, offshoring) and enhance finance capabilities.Manage stakeholder relationships across headquarters, regional teams, joint venture partners, and external entities.What We Are Looking ForContinuous improvement mindset: a thoughtful improvement mindset—curious about how work gets done and motivated to make meaningful, sustainable improvements over time.Leadership expectation: people who consistently put customers first, lead by example with respect for people, deliver results with integrity, and drive continuous improvement by solving problems at the root, developing people, and raising standards every day.Master’s degree in Finance, Accounting, or Business Economics, with a professional qualification (ACCA, CPA, RA, or equivalent preferred).Significant experience (15+ years) in finance leadership roles, including business partnering or controlling at business unit or group level.Strong expertise in financial planning, reporting, accounting systems, and performance management.Strategic mindset with the ability to influence, advise, and support executive decision‑making.Proven leadership skills with experience managing teams and developing finance talent in complex, matrix organisations.Maersk is committed to a diverse and inclusive workplace, and we embrace different styles of thinking. Maersk is an equal‑opportunity employer and welcomes applicants without regard to race, colour, gender, sex, age, religion, creed, national origin, ancestry, citizenship, marital status, sexual orientation, gender identity, genetic information, or any other characteristic protected by applicable law. We will consider qualified applicants with criminal histories in a manner consistent with all legal requirements. We will support your need for any adjustments during the application and hiring process. If you need special assistance or an accommodation to use our website, apply for a position, or to perform a job, please contact us by emailing accommodationrequests@maersk.com.#J-18808-Ljbffr

Senior IT Project Manager - EWM in Pharma Full-time Swiss Delivery Excellence: Transforming Life Science Consulting Worldwide. Fusion Consulting is a globally leading Business and IT boutique consultancy specialized in the Life Sciences industry, partnering with leading companies in pharma, healthcare, and animal health. With over 450 employees and 25 offices worldwide, our mission is to revolutionize our clients' business transformation challenges and set new industry standards through innovative solutions. Focused on S4 HANA, Data & Cloud, and innovative technologies, Fusion Consulting brings unparalleled expertise and commitment to excellence to every project we undertake. Grounded in our commitment to fast and intelligent decision-making, our client-first and open-hearted approach defines our ethos. With unwavering support and an entrepreneurial spirit, our global teamwork transcends boundaries and turns shared visions into reality. We are seeking an experienced Senior IT Project Manager to lead the implementation and optimisation of Extended Warehouse Management (EWM) systems within our pharmaceutical operations. This is a pivotal role that combines technical expertise with strategic project leadership, requiring a professional who can navigate complex regulatory environments whilst delivering transformational warehouse management solutions. Responsibilities Lead the planning, execution, and closure of EWM system implementation projects, ensuring delivery within scope, budget, and timeline constraints. Manage stakeholder communications across multiple departments and external partners, maintaining transparency and managing expectations throughout the project lifecycle. Develop comprehensive project plans, including resource allocation, risk mitigation strategies, and contingency measures specific to pharmaceutical operations. Oversee the configuration, testing, and deployment of EWM solutions, ensuring compliance with pharmaceutical regulatory requirements (Gx P, GDP). Direct and mentor project teams, fostering collaboration and accountability whilst maintaining high standards of technical excellence. Analyse business requirements and translate them into technical specifications, working closely with IT architects and warehouse operations teams. Manage project budgets, procurement processes, and vendor relationships to optimise cost-effectiveness. Facilitate change management activities, ensuring smooth transition and user adoption of new systems. Required Experience and Skills Minimum 8 years' experience in IT project management, with at least 5 years leading EWM or warehouse management system implementations. Proven expertise in SAP EWM systems, including configuration, customisation, and deployment. Strong knowledge of pharmaceutical industry operations, regulatory frameworks (Gx P, GDP), and compliance requirements. Demonstrated ability to manage complex, multi-phase projects with budgets exceeding €1 million. Excellent people skills and proven track record of leading high-performing teams. Advanced proficiency in project management methodologies (Agile, Waterfall, or hybrid approaches). Strong analytical and problem-solving capabilities with meticulous attention to detail. Proficiency in project management tools (MS Project, Jira, or equivalent). Excellent written and verbal communication skills in English; ability to present to senior stakeholders. Desirable Skills and Experience SAP EWM or change management certification, or equivalent professional qualification. Experience with warehouse automation technologies, system integration, and API management. Fluency in English language. Background in pharmaceutical manufacturing, distribution, or supply chain environments. #J-18808-Ljbffr

En Insud Pharma , buscamos incorporar un/a Study Coordinator para un ensayo clínico fase III en el área de salud de la mujer.

About the Role We are seeking a Technical Project Manager to support software delivery initiatives for a leading pharmaceutical company’s R&D platforms and application development programs. Experience within Life Sciences or Pharmaceutical environments is advantageous.

External Account Manager Pharma – BarcelonaBrenntag, global leader in the distribution of chemicals and ingredients, is looking for an External Account Manager Pharma to join our Pharma division in Barcelona.This is a great opportunity to take ownership of key accounts, drive business growth and build long-term relationships within a dynamic and international environment.🚀 Your responsibilitiesAs part of our Pharma team, you will:Develop and grow existing key accounts (Gold / Silver / Bronze), maximizing sales through cross-selling and value-based pricingIdentify new business opportunities and convert prospects into long-term customersPlan and execute customer visits, manage negotiations and close commercial agreementsRespond to RFQs and prepare tailored commercial proposalsAnalyze customer potential and define actionable growth plansLead and coordinate customer-related projects and initiativesMaintain CRM (Salesforce) and ensure accurate reporting🎯 Your profileWe are looking for a commercial and proactive professional with:Degree in Life Sciences (Pharmacy, Chemistry or similar)Minimum 2 years of experience in sales (ideally in pharma, chemicals or related industry)Strong communication and negotiation skillsFluent English and Catalan (written and spoken)Knowledge of Salesforce, SAP or similar tools is a plus💼 What we offerAt Brenntag Spain, you will be part of a global and solid company where your contribution has real impact. We offer:Permanent contract in a leading international companyCareer development and internal growth opportunitiesContinuous training in a professional environmentFlexible working hours and hybrid work modelCompetitive salary + benefits package (meal vouchers, private health insurance, etc.)A collaborative culture focused on safety, respect and diversity🌍 Diversity & InclusionAt Brenntag, we are committed to creating an inclusive environment where everyone feels valued and respected. We welcome applications from all backgrounds and promote equal opportunities for all.Brenntag TA Team

Eres el motor que las Farmacias de Baleares necesitan? 🌟 GPV Pharma - Mallorca & Ibiza Si cuando entras en una farmacia no puedes evitar fijarte en si el escaparate está recto, si el lineal brilla o si el producto estrella está donde toca.

REQUIRED EDUCATION AND EXPERIENCE** University degree in a relevant discipline (ie digital marketing, business administration, scientific) At least 8 years of proven experience in digital strategy, omnichannel marketing and/or e-commerce, preferably within healthcare, pharma or FMCG sectors. Cross

REQUIRED EDUCATION AND EXPERIENCE** University degree in a relevant discipline (ie digital marketing, business administration, scientific) At least 8 years of proven experience in digital strategy, omnichannel marketing and/or e-commerce, preferably within healthcare, pharma or FMCG sectors. MARKE

Global Study Associate ManagerBarcelona,, SpainApply NowFind out how well you match with this jobThe Global Study Associate Manager (GSAM) is a role within Development Operations and is a member of the global study team supporting the delivery of clinical studies from Clinical Study Protocol (CSP) development through study set-up, maintenance, close-out, development of the Clinical Study Report (CSR), and study archiving.The GSAM works with internal and external partners to deliver delegated aspects of the clinical study.Si desea saber un poco más sobre esta oportunidad, o está considerando presentar su candidatura, por favor, lea la siguiente información del puesto.Responsibilities include assisting global study teams, leading administrative activities, overseeing systems for compliance tracking, and providing support for vendor oversight.Studies may be across various therapeutic areas and all phases (I–IV), (including Late Phase, Non-Interventional Studies, Post Authorization Safety Studies, Registries, Early Access Programs, And other study types)## ## You will be responsible for: In collaboration with the global study team (GPD, GSAD, GSMs), other ARDU stakeholders, and key vendors, support activities for clinical study execution, ensuring adherence to timelines and quality standards. Take a leading role in preparing study documents and documents related to key vendors, such as the Vendor Oversight Plan. Actively maintain and facilitate interactions with cross-functional team members, including Data Management, Procurement, Regulatory, Patient Safety, and Quality Assurance. Collaborate closely with both internal and external partners to effectively execute delegated aspects of the clinical study, ensuring alignment with the objectives set by the GPD, GSAD, or GSM. Actively contribute to the planning and execution of both internal and external meetings. Take a proactive role in identifying risks and issues and contribute to the development of mitigation and action plans. Provide support to the GSM in project and budget management, adhering to agreed-upon delegation. Actively participate in or take a leadership role in departmental initiatives and/or Subject Matter Expert (SME) functions. Serve as a mentor and guide for team members, promoting their professional development and cultivating a collaborative work environment. Provide support for other study and functional activities as assigned.## ## You will need to have: Bachelor's degree or equivalent in one of the disciplines related to clinical practice/health care, life sciences, or drug development, or equivalent work experience. Proficiency with technological systems, including Microsoft Office (Excel, PowerPoint, SharePoint Online), eTMF, and Veeva Systems. Excellent organizational, communication, and time management skills. Highly proactive and willing to take initiative. Strong relationship-building skills. The duties of this role are generally conducted in an office environment.## ## We would prefer for you to have: More than 3 years of experience supporting global study teams in a clinical research environment. Ability to drive discussions around the scope of work and oversee vendor-related activities. Excellent knowledge of Essential Documents, CFR, and/or ICH-GCP. Demonstrated ability to collaborate effectively while also working independently.* Project management skills and knowledge of basic project management methodologies.Date Posted21-jul-2026Closing Date10-ago-2026Alexion is proud to be an Equal Employment Opportunity and Affirmative Action employer.We are committed to fostering a culture of belonging where every single person can belong because of their uniqueness.The Company will not make decisions about employment, training, compensation, promotion, and other terms and conditions of employment based on race, color, religion, creed or lack thereof, sex, sexual orientation, age, ancestry, national origin, ethnicity, citizenship status, marital status, pregnancy, (including childbirth, breastfeeding, or related medical conditions), parental status (including adoption or surrogacy), military status, protected veteran status, disability, medical condition, gender identity or expression, genetic information, mental illness or other characteristics protected by law.Alexion provides reasonable accommodations to meet the needs of candidates and employees. xhfqzwm To begin an interactive dialogue with Alexion regarding an accommodation, please contact Alexion participates in E-Verify.#J-18808-Ljbffr

The 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 discrimina

En BESIDE apostamos por el mejor talento dentro del sector tecnológico. Contamos con una unidad de Selección Especializada en perfiles de Ingeniería para incorporarse en la plantilla de nuestros clientes. Trabajamos con un amplio rango de empresas, que nos permitirá encontrarte el puesto que más se ajuste a tus necesidades e intereses profesionales. Te podrás incorporar en las empresas más innovadoras, ofreciéndote proyectos punteros dentro de las ramas de I+D, automoción, pharma, diseño de maquinaria, desarrollo de producto, etc. Para presentar una candidatura, simplemente lea la siguiente descripción del puesto y asegúrese de adjuntar los documentos pertinentes. Seleccionamos un/aTécnico Mecánico de Montaje que formará parte del Departamento de Ingeniería. Será responsable del montaje de maquinaria y componentes mecánicos, así como de la instalación y puesta en marcha de nueva maquinaria, pruebas internas de las máquinas, ajustes y mantenimiento preventivo y correctivo. ¿Qué haré? Estas serán tus funciones principales: Reportando al Responsable del Departamento de Ingeniería, te encargarás de: • Montaje y ajuste de maquinaria, • Instalación y puesta en marcha de nuevas máquinas, • Ajustes internos y pruebas de las máquinas antes de su envío a los clientes, • Intervenciones técnicas en las instalaciones del cliente para localizar y solucionar problemas de impresión, • Mantenimiento preventivo y correctivo de las máquinas Beneficios que tendrás en tu lugar de trabajo: • Contratación directa y de carácter indefinido con cliente final., • Proyecto estable., • Oportunidades de crecimiento profesional., • Modelo de trabajo: presencial. xcskxlj, • Horario: de lunes a viernes de 8h a 17h., • Salario competitivo a convenir según experiencia y conocimientos aportados por el/la candidato/a. #J-18808-Ljbffr

En BESIDE apostamos por el mejor talento dentro del sector tecnológico. Contamos con una unidad de Selección Especializada en perfiles de Ingeniería para incorporarse en la plantilla de nuestros clientes. Trabajamos con un amplio rango de empresas, que nos permitirá encontrarte el puesto que más se ajuste a tus necesidades e intereses profesionales. Te podrás incorporar en las empresas más innovadoras, ofreciéndote proyectos punteros dentro de las ramas de I+D, automoción, pharma, diseño de maquinaria, desarrollo de producto, etc. Para presentar una candidatura, simplemente lea la siguiente descripción del puesto y asegúrese de adjuntar los documentos pertinentes. Seleccionamos un/aTécnico Mecánico de Montaje que formará parte del Departamento de Ingeniería. Será responsable del montaje de maquinaria y componentes mecánicos, así como de la instalación y puesta en marcha de nueva maquinaria, pruebas internas de las máquinas, ajustes y mantenimiento preventivo y correctivo. ¿Qué haré? Estas serán tus funciones principales: Reportando al Responsable del Departamento de Ingeniería, te encargarás de: • Montaje y ajuste de maquinaria, • Instalación y puesta en marcha de nuevas máquinas, • Ajustes internos y pruebas de las máquinas antes de su envío a los clientes, • Intervenciones técnicas en las instalaciones del cliente para localizar y solucionar problemas de impresión, • Mantenimiento preventivo y correctivo de las máquinas Beneficios que tendrás en tu lugar de trabajo: • Contratación directa y de carácter indefinido con cliente final., • Proyecto estable., • Oportunidades de crecimiento profesional., • Modelo de trabajo: presencial. xcskxlj, • Horario: de lunes a viernes de 8h a 17h., • Salario competitivo a convenir según experiencia y conocimientos aportados por el/la candidato/a. #J-18808-Ljbffr

Máyla Pharma busca un/a Director Nacional de Ventas para liderar la estrategia comercial a nivel nacional y acelerar el crecimiento de la compañía en Consumer Healthcare. Reportará a la Dirección y gestionará un equipo formado por delegados y Area Managers, supervisando presupuesto, KPIs y pla

En BESIDE apostamos por el mejor talento dentro del sector tecnológico. Contamos con una unidad de Selección Especializada en perfiles de Ingeniería para incorporarse en la plantilla de nuestros clientes. Trabajamos con un amplio rango de empresas, que nos permitirá encontrarte el puesto que más se ajuste a tus necesidades e intereses profesionales. Te podrás incorporar en las empresas más innovadoras, ofreciéndote proyectos punteros dentro de las ramas de I+D, automoción, pharma, diseño de maquinaria, desarrollo de producto, etc. Experiencia, cualificaciones y habilidades interpersonales, ¿tiene todo lo necesario para triunfar en esta oportunidad? Descúbralo a continuación. Actualmente seleccionamos un/a Senior Executive – HR & Admin para uno de nuestros principales clientes, una empresa internacional líder en la fabricación de maquinaria de impresión para el mercado de etiquetas, envases flexibles, cartón, impresión de seguridad, impresión comercial y prospectos farmacéuticos, entre otros. ¿Qué haré? Estas serán tus funciones principales: • Reclutamiento y Selección, • Relaciones con los empleados, • Gestión del desempeño, • Políticas y cumplimiento de recursos humanos, • Aprendizaje y desarrollo, • Funciones Administrativas, • Informes y análisis de recursos humanos Beneficios que tendrás en tu lugar de trabajo • Contratación directa y de carácter indefinido con cliente final., • Proyecto estable., • Oportunidades de crecimiento profesional., • Modelo de trabajo: presencial., • Horario: de lunes a viernes de 8h a 17h., • Salario competitivo a convenir según experiencia y conocimientos aportados por el/la candidato/a. Requisitos • MBA en Recursos Humanos de un instituto de renombre, • Experiencia en el manejo independiente de algunos de los sistemas de recursos humanos., • Preferiblemente 4 a 6 años de experiencia en RRHH., • Experiencia trabajando en HRIS. xcskxlj Habilidades • Español e inglés fluidos Ubicación • El puesto se desarrollará en Barcelona, España. MARTORELLES #J-18808-Ljbffr

También se abre la posibilidad a poder desempeñar labores comerciales presenciales como consecuencia de buenos resultados y proyección profesional. Comercial (venta telefónica y presencial) Pharma (H/M/X) /h3pDesde Manpower Professional Recruitment estamos gestionando un proyecto de selección m

Manpower Team Empresa De Trabajo Temporal SA busca un Comercial (H/M/X) para ventas telefónicas y presencia en Cerdanyola del Vallés.Los candidatos deben tener experiencia en la venta telefónica de productos del sector Pharma, así como una actitud positiva y proactiva.Se ofrecen buenas condicion

Únete a nuestro equipo como Gestor Comercial Pharma ¿Te apasiona la comunicación y el trato con el cliente? ¿Te gustaría formar parte de un proyecto con una de las compañías farmacéuticas más reconocidas del sector? Buscamos un/a Gestor Comercial Pharma para dar soporte a un laboratorio lí

Aportar visión de industria farmacéutica : al diseño de servicios y propuesta de valor del grupo hacia sus clientes (laboratorios), trasladando el conocimiento de cómo opera medical affairs/marketing científico en pharma.

Promote pharmaceutical products and medical devices to physicians, pharmacists, hospitals, clinics, and healthcare providers. The Medical Sales Representative will be responsible for promoting and selling the company's pharmaceutical products and medical devices to healthcare professionals, pharmaci

Qualifications and Skills* Essential**: Master’s degree in a scientific discipline; Bachelor’s degree with extensive Medical Affairs experience considered; Significant experience in Medical Affairs within the pharmaceutical industry; Demonstrated project and relationship management skills, i

PQE Group is seeking an experienced Pharma Compliance Support Consultant in Barcelona to support pharmaceutical clients in ensuring compliance with global regulatory requirements and drive continuous improvement of Quality Management Systems (QMS).