Regulatory Affairs Documentation Specialist

Improve the Future of Healthcare with GrifolsGrifols is a global healthcare company dedicated to improving the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine, developing, producing, and marketing innovative medicines, solutions, and services in over 110 countries and regions.Join Our Team...

At DSM Nutritional Products, we are seeking a skilled Regulatory Affairs Documentation Specialist to join our team in Barcelona. As a key member of our Regulatory Affairs Documentation Department, you will play a crucial role in collecting and preparing regulatory information for our customers worldwide.Your responsibilities will include providing technical...

Regulatory Affairs Documentation SpecialistWe are seeking a highly skilled Regulatory Affairs Documentation Specialist to join our Biopharma Regulatory department at Grifols, S.A. This is a fantastic opportunity to work with a global healthcare company that has been improving the health and well-being of people around the world since 1909.Key...

Regulatory Affairs Documentation TeamDSM is seeking a skilled Regulatory Affairs Documentation Specialist to join our team in the Regulatory Affairs Documentation Department. As a key member of our team, you will be responsible for collecting and maintaining regulatory information concerning our products for dsm-firmenich customers worldwide.Key...

Regulatory Affairs Documentation RoleAre you interested in working with regulatory information and documents? This position in the Regulatory Affairs Documentation Department involves collecting and organizing regulatory data for DSM-Firmenich customers worldwide.Key Responsibilities• Provide technical support to the Flavor Documentation team• Prepare...

Regulatory Documentation RoleAt DSM, we are seeking a highly organized and detail-oriented individual to join our Regulatory Affairs Documentation Department as a Regulatory Apprentice.Key ResponsibilitiesAs a Documentation Specialist, you will be responsible for providing technical support to the Flavor Documentation team, preparing standard documents and...

About the RoleAt DSM Nutritional Products, we are seeking a skilled Regulatory Affairs Documentation Specialist to join our team. As a key member of our Documentation Department, you will play a vital role in collecting and organizing regulatory information related to our products. This information is crucial for our customers to comply with applicable...

At Dsm Nutritional Products, we are looking for a Regulatory Affairs Specialist to join our team in Barcelona. In this role, you will be responsible for providing technical support to the Perfumery and Beauty Documentation team.Key responsibilities include preparing standard documents and basic questionnaires for worldwide customers, using our internal...

Job Title: Regulatory Affairs SpecialistJob Summary:We are seeking a highly skilled Regulatory Affairs Specialist to join our team at Alk-Abelló A/S. As a Regulatory Affairs Specialist, you will be responsible for handling regulatory CMC documentation of products manufactured at our site in Madrid, for worldwide submissions. You will also be responsible for...

About DSM Nutritional ProductsWe are a leading company in the development of nutritional products. Our goal is to create innovative solutions that improve people's health and well-being.Job DescriptionAs a Regulatory Affairs Documentation Specialist, you will be responsible for providing technical support to the Perfumery and Beauty Documentation team. You...

The Regulatory Affairs department at Werfen is seeking a highly skilled Quality and Regulatory Affairs specialist to join our team in Barcelona, Spain.As a Quality and Regulatory Affairs specialist, you will be responsible for supporting the execution of pre and post-market regulatory affairs departmental functions. This includes assisting in the preparation...

OverviewWerfen is seeking a Regulatory Affairs Specialist to support the execution of pre- and post-market regulatory affairs departmental functions. The ideal candidate will assist in the preparation of documentation and information required to place and keep products on the market, including regulatory submissions, licensing and registrations. Key...

Job Title:Regulatory Affairs SpecialistGalderma Pharma S.A is seeking a highly skilled Regulatory Affairs Specialist to join our team. As a Regulatory Affairs Specialist, you will be responsible for delivering innovative, breakthrough global regulatory strategies for clinical trial registration with health authorities.The ideal candidate will have a strong...

About FARMAPROJECTS SAUFARMAPROJECTS SAU is a B2B Pharmaceutical Laboratory company offering a broad Portfolio of Generic Pharmaceutical Products and Value Added Medicines.We are looking for a new Regulatory Affairs Senior Specialist to join our Regulatory Affairs Department and contribute to the business.About the RoleAs a Regulatory Affairs Senior...

Join a dynamic and growing affiliate in Barcelona, Spain, as a Regulatory Affairs Documentation Apprentice. This exciting role offers the opportunity to introduce you to our products' documentation world, one of the crucial steps to get our customers' approval for sales.We are looking for recent graduates in Chemistry, Biology, Pharmacy or another related...

Regulatory Affairs SpecialistAt Ramboll Group A/S, we are seeking a highly skilled Regulatory Affairs Specialist to join our international Health Sciences service line. As a key member of our team, you will be responsible for providing technical support to clients and colleagues on issues relating to product regulatory compliance and stewardship in Spain.Key...

Improve the Future of Healthcare with GrifolsGrifols is a global healthcare company dedicated to improving the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine, developing, producing, and marketing innovative medicines, solutions, and services in over 110 countries and regions.We are...

Key Responsibilities:As a Regulatory Affairs Documentation Manager, you will spearhead the planning, execution, and successful delivery of projects involving multiple stakeholders. This dynamic role demands leadership of cross-functional teams, meticulous management of project timelines and resources, and a steadfast commitment to delivering projects on...

Job Title: Regulatory Affairs Specialist - EBDJob Summary: We are seeking a highly skilled Regulatory Affairs Specialist to manage the global product registration and regulatory approvals for our Energy-Based Devices (EBD).Key Responsibilities:* Ensure compliance with international regulatory authorities* Support market entry for EBDs worldwide* Collaborate...

Job SummaryWe are seeking a highly skilled Senior Packaging Regulatory Affairs Specialist to join our Biopharma Regulatory department at Grifols Sa. This role will be responsible for preparing, reviewing, and following up on documentation generated at the Regulatory Affairs department or needed for a regulatory submission.Key ResponsibilitiesPrepare, review,...