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BELIEVE IN LIFE. Join a company that takes you further! Galenicum is one of the fastest growing companies in the pharmaceutical sector! We are enthusiastic about life, devoting our talent and effort to providing high-quality affordable pharmaceuticals worldwide. People are the key to our present and future success, so we carefully select candidates that meet the requirements for each position, however most importantly, who also fit with our cultural DNA and values. Here’s the lowdown on what your role will actually look like (spoiler alert: it’s awesome!) We are looking for a Regulatory Affairs Expert to join our Regulatory Affairs Team! What you'll be rocking: • Compilation, evaluation and submission of complete registration dossiers to specific regulatory agencies, of both, internal development and in-licensing products; under other RA team senior associate supervision. Contact with suppliers and clients, as needed, in order to obtain a dossier that meets the requirements of the country of destination., • Support in developing and writing clear arguments and explanations for deficiency letters., • Maintenance of approved dossiers and RA internal databases. Monitoring, updating and adapting documents, preparing submissions of variations and renewals to strict deadlines; under other RA team senior associate supervision., • Compilation and Evaluation of ASMF., • Writing clear, accessible product labels and patient information leaflets., • Review of marketing materials., • Audit or feasibility checks of dossiers to be registered in the required markets and coordination of the audits of the region., • Be updated on the regulatory requirements (EU, national and/or international legislation, as applicable, guidelines and customer practices) and registration procedures in all the company's export markets. What you bring to the table: • Minimum between 6 months to 1 year experience in the area of registration of medicines for human use in the European Union and/or International markets, preferably generic drugs., • Very valuable to have experience in requirements in other markets. Educational milestone: • Bachelor's degree in Medicine or Pharmacy, or other health sciences., • Preferably Master's degree in Regulatory Affairs., • Excellent level of scientific and business English, spoken and written., • Excellent computer skills. Your key superpowers: • Highly disciplined, responsible, methodical, resolutive and organized individual., • Excellent oral and written communication and interpersonal skils., • Strong attention to detail and analytical frame of mind., • Understanding of both legal and scientific matters., • Capable to work under pressure and to strict deadlines, under your own initiative whilst being a good team player., • Able to find strategies according to legislation to solve problems and proposed innovative solutions for regulatory submissions., • Ability to prioritize multiple tasks. What makes Galenicum a top-tier workplace? • A challenging company, and a dynamic team to work with., • A Workspace to enjoy. Pleasant, sustainable, and architecture-awarded office., • A flexible schedule to match your preferences and workload., • A training offer to learn beyond your job with a broad set of topics: Galenicum Laude., • Health insurance coverage to feel cared., • Food to keep your energy up. Subsidized meals in our office restaurant Popina., • Gym to help you maintain a healthy lifestyle., • Flexible remuneration., • And, very important! A Buddy to help you land smoothly in our company since day 1. We’re looking for someone who works hard, plays hard, and laughs harder. Sound like you? Come aboard. Believe in life

🚨 NEW OPPORTUNITY – Temporary QA Specialist (Pharma) 📍 On-site | Sant Cugat (Barcelona) 📅 Contract: End May 2026 – December 2026 Oxford Global Resources – Life Sciences Unit is supporting one of the fastest-growing pharmaceutical companies headquartered in Spain, recognized for its strong commitment to innovation and R&D excellence. We are currently looking for an experienced QA R&D Specialist to join their Quality Assurance – Pharmaceutical Development team on a temporary basis. 🔬 Role: QA Specialist – R&D (GMP, IMPs, Quality Systems) 📍 Location: Sant Cugat (on-site) 📅 Start: ASAP | 🕐 Full-time, long-term project 💼 Experience: Minimum 3–4 years in a similar QA R&D GMP role 📈 Sector: Pharmaceutical | GxP | Clinical Trials | IMPs 🧪 Main Responsibilities ✔️ Review and/or approval of key GMP documentation generated by the Pharmaceutical Development area, including: • Manufacturing, packaging, and labeling instructions for IMPs, • Analytical methods, specifications (LIMS), and specification dossiers, • ICH stability protocols/reports, • Method validation documentation, • Shelf-life justification reports for IMPs, • Deviation and change control management, • Master Manufacturing Plans (MMP & MMPr), • SOPs for equipment cleaning, operations, and room procedures, • Deviation handling, CAPAs, change controls, complaints, • Investigations of OOS, OOE, OOT and related CAPA evaluation, • Edition and maintenance of Quality Agreements, • SOPs and controlled documents related to Quality & R&D ✔️ Participate in audits (internal/external) and inspections ✔️ Manage submissions to AEMPS as needed (manufacturing/import/export, controlled substances) ✅ Your Profile • Bachelor’s or Master’s degree in Pharmacy, Chemistry, Biotechnology, or similar, • 3–5 years of experience in QA within an R&D or IMPs-focused GMP environment, • Solid knowledge of ICH, GxP, EU GMP Annex 13, • Experience working closely with manufacturing, analytical, and regulatory teams, • Spanish required; English professional level, • Team player with attention to detail and problem-solving mindset 🌟 What’s in it for you? ✅ Join a highly dynamic team in a company with a strong pipeline and innovative product portfolio ✅ Work on-site in Sant Cugat, in close collaboration with R&D, QA, and Regulatory teams ✅ Be part of a mission-driven, growth-oriented pharma company Interested? Apply now or reach out to our Life Sciences team at Oxford Global Resources to learn more: #LifeSciences #GMP #QAJobs #IMPs #PharmaJobs #SantCugat #BarcelonaJobs #OxfordGlobalResources

Estamos buscando un BUSINESS DEVELOPMENT del sector farmacéutico para formar parte de nuestra empresa líder del sector y en plena expansión. Company Description Labiana Pharmaceuticals has extensive expertise in contract manufacturing services for the human pharmaceutical industry, collaborating with prominent multinational companies. Operating under an EU-GMP certificate, Labiana Pharmaceuticals manages a state-of-the-art production facility with a strong focus on tablet manufacturing, film coating technology (FCT), and comprehensive packaging capabilities across seven packaging lines. The company has registered numerous marketing authorizations globally, offering integrated services that span drug development from concept to production and commercialization. Supported by a highly skilled team in Technical, Regulatory Affairs, and Research and Development departments, Labiana is committed to delivering high-quality solutions for its clients. Role Description This is a full-time, on-site Business Development (Licensing Out) role based in Barcelona. The role involves spearheading licensing-out strategies, identifying and pursuing potential business opportunities, conducting market research and lead generation, and establishing partnerships to expand the company's reach. Additionally, the role includes maintaining strong relationships with clients, managing key accounts, and collaborating with internal teams to align strategic objectives with business goals. Qualifications • Strong Analytical and Market Research skills to identify trends, assess opportunities, and support strategic decision-making., • Excellent Communication and Customer Service skills to effectively engage with clients and stakeholders., • Proven experience in Lead Generation and building long-term business relationships., • Relevant knowledge of licensing and business development within the pharmaceutical industry is an advantage., • Bachelor’s degree in Business, Marketing, Life Sciences, or a related field is preferred., • Proficiency in English; additional languages are considered an asset., • Ability to work collaboratively with cross-functional teams and meet challenging deadlines within a dynamic environment. Contrato: Estable Salario: Según perfil. Beneficios sociales: Seguro médico Adeslas, seguro de vida, bonificación 50% comida, fruta en la oficina, clases de inglés, bonos/ayudas a los empleados, etc.

BELIEVE IN LIFE. Join a company that takes you further! Galenicum is one of the fastest growing companies in the pharmaceutical sector! We are enthusiastic about life, devoting our talent and effort to providing high-quality affordable pharmaceuticals worldwide. People are the key to our present and future success, so we carefully select candidates that meet the requirements for each position, however most importantly, who also fit with our cultural DNA and values. Here’s the lowdown on what your role will actually look like (spoiler alert: it’s awesome!) We are looking for a Regulatory Affairs Expert to join our Regulatory Affairs Team! What you'll be rocking: • Compilation, evaluation and submission of complete registration dossiers to specific regulatory agencies, of both, internal development and in-licensing products; under other RA team senior associate supervision. Contact with suppliers and clients, as needed, in order to obtain a dossier that meets the requirements of the country of destination., • Support in developing and writing clear arguments and explanations for deficiency letters., • Maintenance of approved dossiers and RA internal databases. Monitoring, updating and adapting documents, preparing submissions of variations and renewals to strict deadlines; under other RA team senior associate supervision., • Compilation and Evaluation of ASMF., • Writing clear, accessible product labels and patient information leaflets., • Review of marketing materials., • Audit or feasibility checks of dossiers to be registered in the required markets and coordination of the audits of the region., • Be updated on the regulatory requirements (EU, national and/or international legislation, as applicable, guidelines and customer practices) and registration procedures in all the company's export markets. What you bring to the table: • Minimum between 6 months to 1 year experience in the area of registration of medicines for human use in the European Union and/or International markets, preferably generic drugs., • Very valuable to have experience in requirements in other markets. Educational milestone: • Bachelor's degree in Medicine or Pharmacy, or other health sciences., • Preferably Master's degree in Regulatory Affairs., • Excellent level of scientific and business English, spoken and written., • Excellent computer skills. Your key superpowers: • Highly disciplined, responsible, methodical, resolutive and organized individual., • Excellent oral and written communication and interpersonal skils., • Strong attention to detail and analytical frame of mind., • Understanding of both legal and scientific matters., • Capable to work under pressure and to strict deadlines, under your own initiative whilst being a good team player., • Able to find strategies according to legislation to solve problems and proposed innovative solutions for regulatory submissions., • Ability to prioritize multiple tasks. What makes Galenicum a top-tier workplace? • A challenging company, and a dynamic team to work with., • A Workspace to enjoy. Pleasant, sustainable, and architecture-awarded office., • A flexible schedule to match your preferences and workload., • A training offer to learn beyond your job with a broad set of topics: Galenicum Laude., • Health insurance coverage to feel cared., • Food to keep your energy up. Subsidized meals in our office restaurant Popina., • Gym to help you maintain a healthy lifestyle., • Flexible remuneration., • And, very important! A Buddy to help you land smoothly in our company since day 1. We’re looking for someone who works hard, plays hard, and laughs harder. Sound like you? Come aboard. Believe in life

BELIEVE IN LIFE. Join a company that takes you further! Galenicum is one of the fastest growing companies in the pharmaceutical sector! We are enthusiastic about life, devoting our talent and effort to providing high-quality affordable pharmaceuticals worldwide. People are the key to our present and future success, so we carefully select candidates that meet the requirements for each position, however most importantly, who also fit with our cultural DNA and values. Here’s the lowdown on what your role will actually look like (spoiler alert: it’s awesome!) We are looking for a Regulatory Affairs Expert to join our Regulatory Affairs Team! What you'll be rocking: • Compilation, evaluation and submission of complete registration dossiers to specific regulatory agencies, of both, internal development and in-licensing products; under other RA team senior associate supervision. Contact with suppliers and clients, as needed, in order to obtain a dossier that meets the requirements of the country of destination., • Support in developing and writing clear arguments and explanations for deficiency letters., • Maintenance of approved dossiers and RA internal databases. Monitoring, updating and adapting documents, preparing submissions of variations and renewals to strict deadlines; under other RA team senior associate supervision., • Compilation and Evaluation of ASMF., • Writing clear, accessible product labels and patient information leaflets., • Review of marketing materials., • Audit or feasibility checks of dossiers to be registered in the required markets and coordination of the audits of the region., • Be updated on the regulatory requirements (EU, national and/or international legislation, as applicable, guidelines and customer practices) and registration procedures in all the company's export markets. What you bring to the table: • Minimum between 6 months to 1 year experience in the area of registration of medicines for human use in the European Union and/or International markets, preferably generic drugs., • Very valuable to have experience in requirements in other markets. Educational milestone: • Bachelor's degree in Medicine or Pharmacy, or other health sciences., • Preferably Master's degree in Regulatory Affairs., • Excellent level of scientific and business English, spoken and written., • Excellent computer skills. Your key superpowers: • Highly disciplined, responsible, methodical, resolutive and organized individual., • Excellent oral and written communication and interpersonal skils., • Strong attention to detail and analytical frame of mind., • Understanding of both legal and scientific matters., • Capable to work under pressure and to strict deadlines, under your own initiative whilst being a good team player., • Able to find strategies according to legislation to solve problems and proposed innovative solutions for regulatory submissions., • Ability to prioritize multiple tasks. What makes Galenicum a top-tier workplace? • A challenging company, and a dynamic team to work with., • A Workspace to enjoy. Pleasant, sustainable, and architecture-awarded office., • A flexible schedule to match your preferences and workload., • A training offer to learn beyond your job with a broad set of topics: Galenicum Laude., • Health insurance coverage to feel cared., • Food to keep your energy up. Subsidized meals in our office restaurant Popina., • Gym to help you maintain a healthy lifestyle., • Flexible remuneration., • And, very important! A Buddy to help you land smoothly in our company since day 1. We’re looking for someone who works hard, plays hard, and laughs harder. Sound like you? Come aboard. Believe in life

BELIEVE IN LIFE. Join a company that takes you further! Galenicum is one of the fastest growing companies in the pharmaceutical sector! We are enthusiastic about life, devoting our talent and effort to providing high-quality affordable pharmaceuticals worldwide. People are the key to our present and future success, so we carefully select candidates that meet the requirements for each position, however most importantly, who also fit with our cultural DNA and values. Here’s the lowdown on what your role will actually look like (spoiler alert: it’s awesome!) We are looking for a Regulatory Affairs Expert to join our Regulatory Affairs Team! What you'll be rocking: • Compilation, evaluation and submission of complete registration dossiers to specific regulatory agencies, of both, internal development and in-licensing products; under other RA team senior associate supervision. Contact with suppliers and clients, as needed, in order to obtain a dossier that meets the requirements of the country of destination., • Support in developing and writing clear arguments and explanations for deficiency letters., • Maintenance of approved dossiers and RA internal databases. Monitoring, updating and adapting documents, preparing submissions of variations and renewals to strict deadlines; under other RA team senior associate supervision., • Compilation and Evaluation of ASMF., • Writing clear, accessible product labels and patient information leaflets., • Review of marketing materials., • Audit or feasibility checks of dossiers to be registered in the required markets and coordination of the audits of the region., • Be updated on the regulatory requirements (EU, national and/or international legislation, as applicable, guidelines and customer practices) and registration procedures in all the company's export markets. What you bring to the table: • Minimum between 6 months to 1 year experience in the area of registration of medicines for human use in the European Union and/or International markets, preferably generic drugs., • Very valuable to have experience in requirements in other markets. Educational milestone: • Bachelor's degree in Medicine or Pharmacy, or other health sciences., • Preferably Master's degree in Regulatory Affairs., • Excellent level of scientific and business English, spoken and written., • Excellent computer skills. Your key superpowers: • Highly disciplined, responsible, methodical, resolutive and organized individual., • Excellent oral and written communication and interpersonal skils., • Strong attention to detail and analytical frame of mind., • Understanding of both legal and scientific matters., • Capable to work under pressure and to strict deadlines, under your own initiative whilst being a good team player., • Able to find strategies according to legislation to solve problems and proposed innovative solutions for regulatory submissions., • Ability to prioritize multiple tasks. What makes Galenicum a top-tier workplace? • A challenging company, and a dynamic team to work with., • A Workspace to enjoy. Pleasant, sustainable, and architecture-awarded office., • A flexible schedule to match your preferences and workload., • A training offer to learn beyond your job with a broad set of topics: Galenicum Laude., • Health insurance coverage to feel cared., • Food to keep your energy up. Subsidized meals in our office restaurant Popina., • Gym to help you maintain a healthy lifestyle., • Flexible remuneration., • And, very important! A Buddy to help you land smoothly in our company since day 1. We’re looking for someone who works hard, plays hard, and laughs harder. Sound like you? Come aboard. Believe in life

BELIEVE IN LIFE. Join a company that takes you further! Galenicum is one of the fastest growing companies in the pharmaceutical sector! We are enthusiastic about life, devoting our talent and effort to providing high-quality affordable pharmaceuticals worldwide. People are the key to our present and future success, so we carefully select candidates that meet the requirements for each position, however most importantly, who also fit with our cultural DNA and values. Here’s the lowdown on what your role will actually look like (spoiler alert: it’s awesome!) We are looking for a Regulatory Affairs Expert to join our Regulatory Affairs Team! What you'll be rocking: • Compilation, evaluation and submission of complete registration dossiers to specific regulatory agencies, of both, internal development and in-licensing products; under other RA team senior associate supervision. Contact with suppliers and clients, as needed, in order to obtain a dossier that meets the requirements of the country of destination., • Support in developing and writing clear arguments and explanations for deficiency letters., • Maintenance of approved dossiers and RA internal databases. Monitoring, updating and adapting documents, preparing submissions of variations and renewals to strict deadlines; under other RA team senior associate supervision., • Compilation and Evaluation of ASMF., • Writing clear, accessible product labels and patient information leaflets., • Review of marketing materials., • Audit or feasibility checks of dossiers to be registered in the required markets and coordination of the audits of the region., • Be updated on the regulatory requirements (EU, national and/or international legislation, as applicable, guidelines and customer practices) and registration procedures in all the company's export markets. What you bring to the table: • Minimum between 6 months to 1 year experience in the area of registration of medicines for human use in the European Union and/or International markets, preferably generic drugs., • Very valuable to have experience in requirements in other markets. Educational milestone: • Bachelor's degree in Medicine or Pharmacy, or other health sciences., • Preferably Master's degree in Regulatory Affairs., • Excellent level of scientific and business English, spoken and written., • Excellent computer skills. Your key superpowers: • Highly disciplined, responsible, methodical, resolutive and organized individual., • Excellent oral and written communication and interpersonal skils., • Strong attention to detail and analytical frame of mind., • Understanding of both legal and scientific matters., • Capable to work under pressure and to strict deadlines, under your own initiative whilst being a good team player., • Able to find strategies according to legislation to solve problems and proposed innovative solutions for regulatory submissions., • Ability to prioritize multiple tasks. What makes Galenicum a top-tier workplace? • A challenging company, and a dynamic team to work with., • A Workspace to enjoy. Pleasant, sustainable, and architecture-awarded office., • A flexible schedule to match your preferences and workload., • A training offer to learn beyond your job with a broad set of topics: Galenicum Laude., • Health insurance coverage to feel cared., • Food to keep your energy up. Subsidized meals in our office restaurant Popina., • Gym to help you maintain a healthy lifestyle., • Flexible remuneration., • And, very important! A Buddy to help you land smoothly in our company since day 1. We’re looking for someone who works hard, plays hard, and laughs harder. Sound like you? Come aboard. Believe in life

Document Specialist I (European Spanish/English). Must be able to read, write, and speak European Spanish fluently. Annual gross salary: EUR 25,060.

Candidates should have a high school diploma or GED, preferably a business or legal assistant certification, and must be fluent in European Spanish. A leading gaming services provider in Sant Cugat del Vallès is seeking a Document Specialist I (European Spanish/English) to support the QA team.

A leading research foundation in Spain is seeking a motivated professional to join its International Projects Management team.Inscríbase ahora, lea los detalles del trabajo desplazándose hacia abajo.Verifique que posee las habilidades necesarias antes de enviar una solicitud.The role involves mana

Tienes experiencia en ventas? ¿Tienes experiencia en mercados internacionales y quieres seguir creciendo como Sales Executive? Si eres una persona con iniciativa, con energía, con ambición para conseguir metas y crecer día a día; si disfrutas con el contacto con el cliente, te gustan las ventas

Tienes experiencia en ventas? ¿Tienes experiencia en mercados internacionales y quieres seguir creciendo como Sales Executive? Si eres una persona con iniciativa, con energía, con ambición para conseguir metas y crecer día a día; si disfrutas con el contacto con el cliente, te gustan las ventas

EU Business School is seeking a.

Tienes experiencia en ventas? ¿Tienes experiencia en mercados internacionales y quieres seguir creciendo como Sales Executive? Si eres una persona con iniciativa, con energía, con ambición para conseguir metas y crecer día a día; si disfrutas con el contacto con el cliente, te gustan las ventas

Réactivité, rigueur, et excellentes compétences relationnelles. Passion pour le développement commercial, l'entrepreneuriat, et la négociation. Formation: Apprenez des meilleurs dans le domaine.

EU Business School is seeking a.

Certification Google Partner: Nos experts sont certifiés et formés pour optimiser vos compétences et vous obtenir les meilleurs résultats !. Réactivité, rigueur, et excellentes compétences relationnelles. Passion pour le développement commercial, l'entrepreneuriat, et la négociation.

Design, build, and maintain EU regional data pipelines and data platforms under. Group data platform framework, supporting European business operations. Assist in integrating EU-local data sources, such as regional partners’ data,.

This position is based fully on-site (no remote) at our EU HQ office (Cornellà de Llobregat, Barcelona). Join a fast-growing global automotive brand expanding across Europe. Work at our European headquarters with exposure to international HR operations.

EU data experience is a plus but not mandatory. Design, build, and maintain EU regional data pipelines and data platforms under. Group data platform framework, supporting European business operations.

Cher futur stagiaire, si vous êtes prêt pour un challenge et désireux de croître dans un environnement stimulant, alors cette place est faite pour vous! 🎯. Certification Google Partner: Nos experts sont certifiés et formés pour optimiser vos compétences et vous obtenir les meilleurs résul

As a Provider Manager in the EU 3P Compliance organization you will join a dynamic team at the forefront of this vision to build a global marketplace.

This is a mid-level role where you will be the strategic high-touch point of reference for our key Enterprise and Mid-Market clients across the European Retail and Grocery sector. We are in a strong scale-up phase rapidly expanding across Europe and Latin America and we are looking for talented indi

A leading dermocosmetic company in Barcelona is seeking a Marketplaces KAM to manage Amazon Seller and Vendor accounts across multiple EU countries.

Develop overseas market strategies, sales strategies, and sales plans for the assigned region in line with the companys overall strategy.Establish and develop the overseas sales team in the assigned region, building a highly capable and cohesive sales force.Expand the overseas market, secure key acc

Buscamos un Consultor económico-fiscal de Proyectos internacionales de I+D, para INCOTEC, grupo empresarial especialista en la gestión de la innovación para empresas privadas, formado por un equipo de más de 130 personas y 9 oficinas, con un crecimiento sostenido desde su arranque en el año 200

Gestionar problemas de postventa con distribuidores del sur de Europa, coordinando con técnicos de los mismos. Handle after-sales issues with distributors in Southern Europe by coordinating with their technical staff, providing technical solutions, and conducting regular after-sales training sessio

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