Regulatory Affairs Specialist CMC

Mission Provide regulatory advice and prepare and maintain the chemical-pharmaceutical regulatory documentation for strategic brands for international and local products, maximising compliance with current guidelines while minimising regulatory commitments. Tasks and Responsibilities Participate in different projects (Pharma and Chemistry) developed by the...

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and...

MissionBe a member of R&D teams to provide an expert DMPK & Bioanalysis support to Large Molecule therapy projects. Implementation and validation of adequate bioanalytical strategies, with focus on PK assays, PD assays and immunogenicity assays, across the project lifecycle in a multidisciplinary environment. Coordinate sample analysis including...

Corporate Head of Regulatory AffairsLocation: Barcelona or remote but open to commute.Job PurposeEnsure that the worldwide regulatory strategies are clearly supported and implemented in the product development, commercialization and life cycle management of the medicinal products.Major AccountabilitiesDevelopment of international regulatory strategies and...

Corporate Head of Regulatory Affairs Location: Barcelona or remote but open to commute. Job Purpose Ensure that the worldwide regulatory strategies are clearly supported and implemented in the product development, commercialization and life cycle management of the medicinal products. Major Accountabilities Development of international...

Mission •    The Global Clinical Program Lead (GCPL) is a core member of the Global Project Team and is leading the Strategic Clinical Team within Global Clinical Development, working cross functionally with other R&D and non-R&D departments such as Regulatory and Patient Safety, Disease Biology, Global Market Access and Pricing, Medical affairs,...

Vantage is a leading supplier of naturally derived specialty ingredients and formulations that cater to the evolving needs of industrial and consumer markets. Through our chemistries, our customer focus and our global footprint, we are ENABLING TOMORROW’S SOLUTIONS TODAY. As a company on the move, you’ll be working as part of a collaborative team...

Why do an intership at Eurofragance?In Eurofragance you will be part of the exciting world of smells and fragrances with our Passion, Performance & Entrepreneurship values.You will grow and learn in a company in constant growth and expansion.You will have the opportunity to develop with top professionals in the sector.You will be part of a Global Company...

Additional Job DescriptionAre you looking for a career in a multinational company? Ecolab is currently seeking a Senior Regulatory Specialist Biocides. This is an office-based role; the candidate may reside near one of our offices in:Vimercate (Italy)Barcelona (Spain)Northwich (UK)Monheim (Germany)Lille (France)Your ResponsibilitiesSet up the regulatory...

 We are ZimVie, a publicly traded, global life sciences leader focused on restoring daily life by advancing clinical technology to improve patients’ smiles, function, and confidence. Our company is founded on a legacy of trusted brands, products, and clinical evidence made possible through an inclusive and collaborative culture that empowers our team...

Requisitos - Experiência mínima de un año en posiciones similares en gestión de calidad y gestión de normativas regulatorias. - Ingles fluido **Competencias/Habilidades**: Capacidad Analítica. Capacidad de Aprendizaje. Comunicación. Colaboración. Flexibilidad. Orientación Cliente. Iniciativa. Planificación. Orientación a...

Additional Job Description Are you looking for a career in a multinational company? Ecolab is currently seeking a Senior Regulatory Specialist Biocides. This is an office-based role; the candidate may reside near one of our offices in: Vimercate (Italy) Barcelona (Spain) Northwich (UK) Monheim (Germany) Lille...

Fecha: 9 may. 2024- Ubicación: SFEL - R&D SANT FELIU DE LLOBR**Mission**: - The Global Clinical Program Lead (GCPL) is a core member of the Global Project Team and is leading the Strategic Clinical Team within Global Clinical Development, working cross functionally with other R&D and non-R&D departments such as Regulatory and Patient Safety, Disease...

Actividades destacadas a realizar: Medical Affairs:Colaboración en todas las actividades relacionadas con las partes clínicas y preclínicas del dossier de registro de medicamentos para productos actuales y potenciales, para registro y para contestar cartas de deficiencias y variaciones regulatorias en distintos territorios. También relacionadas con food...

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and...

Neuraxpharm is a leading European specialty pharmaceutical company focused on the treatment of the central nervous system (CNS), including both psychiatric and neurological disorders. It has a unique understanding of the CNS market built over 35 years. Neuraxpharm is constantly innovating, with new products and solutions to address unmet patient needs and...

Job Description - As a Product Specialist/Expert you evaluate IVD Expert medical products in accordance with European guidelines and standards. You are responsible for the review of the technical documentation of selected product groups in non-active products area in your field of expertise – Sterilize and non-sterilize devices, Implantable devices...

Neuraxpharm is the leading European specialty pharmaceutical company focused on the treatment of the central nervous system (CNS), including both psychiatric and neurological disorders. It has a unique understanding of the CNS market built over 35 years. Neuraxpharm is constantly innovating, with new products and solutions to address unmet patient needs...

As a Product Specialist/Expert you evaluate Non-Active medical products in accordance with European guidelines and standards. You are responsible for the review of the technical documentation of selected product groups in non-active products area in your field of expertise - Sterilize and non-sterilize devices, Implantable devices as orthopedic and dental...

**Site Name**: GSK Tres Cantos, Madrid **Posted Date**: Jul 31 2023 **Therapeutic Area Director, Therapeutic Area Medical Affairs Lead**: As a Director you will play a key role and will be a member of the GSK Pharma Research & Development Unit. The role reports directly into the VP Medical Director, Spain. **_ Job purpose:_** Responsible for all medical...