Life Sciences | Regulatory Affairs Officer

Viatris is seeking an Associate Regulatory Affairs Executive - Central Regulatory Affairs (CRA), Europe. You will support regulatory submissions, maintain product licences, and ensure compliance across multiple European markets.Ideal candidates have a degree in Pharmacy or Life Sciences, fluent English, and 0-2 years in regulatory affairs or a regulated...

Viatris is seeking a Senior Regulatory Affairs Administrator to support regulatory activities across Europe, ensuring compliance with European and local requirements. The role collaborates with internal stakeholders and affiliate teams to maintain marketing authorisations and manage regulatory tasks.The ideal candidate has a solid administrative background...

Devote Consulting seeks a Senior Consultant with expertise in clinical operations, data, and GxP systems to help life sciences clients optimize processes and compliance documentation. You will deliver changes across R&D, clinical operations, and regulatory affairs, guiding projects in a fast-paced consulting environment.You hold a master’s degree in...

Compliance MedQRA is a growing international consultancy providing regulatory affairs and quality assurance services to medical device, SaMD, IVD, pharmaceutical, and life sciences companies.We support clients throughout the product lifecycle, from regulatory strategy and market access to QMS implementation, certification, and post-market compliance.We are...

Devote Consulting actively seeks recent graduates to join a growing team delivering life sciences consulting. You’ll work on projects that improve processes, data, and systems across medical devices, R&D, and regulatory affairs. In this role you’ll contribute to stakeholder management, project planning, and organizational change, gaining hands-on...

Astrum CRO is seeking a Regulatory Affairs & Pharmacovigilance Manager to lead the RA/PV team across clinical trials and client projects. You will ensure regulatory compliance and patient-safety systems, oversee submissions, safety reporting, and sign-off on key study documents.Ideal candidates hold a degree in pharmacy, medicine, or life sciences, with...

Syneos Health, Inc. invites an experienced Senior Regulatory Consultant to join our GRO RPSM portfolio.You will provide global regulatory project management support to a dedicated sponsor and collaborate with Global Regulatory Affairs across regions, including Europe, the UK, and the Americas. Ideal candidates hold a life sciences degree (advanced degree...

Viatris in Lisbon is seeking a RIM Data Maintenance Specialist to provide user support for creating and maintaining records in the Regulatory Information Management system (Veeva Registrations). You will collaborate with Regulatory Affairs on data standards and oversee data cleansing and compliance checks to keep master data accurate. The role is hybrid,...

We are looking for a Regulatory Affairs professional to join our IQVIA Biotech Regulatory Affairs team, supporting clinical research projects across Europe. In this role, you will provide regulatory expertise and hands-on support throughout clinical development, with a particular focus on EU Clinical Trials Regulation (EU CTR) submissions. You will work as...