Regulatory Affairs Specialist – Oncology

MSD in Spain is seeking a Regulatory Affairs Specialist to join our Regulatory Affairs team, driving lifecycle management for Oncology and Vaccines. You will work with local, regional, and global partners and engage with authorities such as AEMPS to ensure compliant and timely patient access to innovative therapies.The ideal candidate has a Life Sciences...

Merck in Spain seeks a Regulatory Affairs Specialist to join our Regulatory Affairs team, focusing on Oncology and Vaccines. You will manage regulatory lifecycle for our product portfolio in Spain, collaborating with local, regional, and global teams, and engaging with health authorities to ensure timely patient access.You will prepare and submit MA...

MSD in Spain is seeking a Regulatory Affairs Specialist to manage regulatory lifecycle for oncology and vaccines portfolios. You will coordinate with local, regional and global teams and engage with AEMPS to ensure timely access to innovative therapies. You will prepare MA applications, manage variations and renewals, and ensure labeling and SmPCs comply...

An amazing opportunity has arisen for a Regulatory Affairs Specialist to join our Regulatory Affairs team in Spain. In this role, you will be part of an experienced and talented team responsible for the regulatory lifecycle management of our assigned product portfolio in Spain, with a dedicated focus on the therapeutic areas of Oncology and Vaccines, as well...

Job Description An amazing opportunity has arisen for a Regulatory Affairs Specialist to join our Regulatory Affairs team in Spain. In this role, you will be part of an experienced and talented team responsible for the regulatory lifecycle management of our assigned product portfolio in Spain, with a dedicated focus on the therapeutic areas of Oncology and...

This job is with MSD, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly.¿Todo listo para enviar su solicitud? Asegúrese de comprender todas las responsabilidades y tareas asociadas a este puesto antes de continuar.Job DescriptionAn amazing...

We are the people who give possibilities purpose BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of MedTech products per...

We are seeking an experienced and proactiveRegulatory Affairs Specialistto join our team. In this role, you will be responsible for preparing, compiling, and submitting technical documentation to secure and maintain global market access for our medical device portfolio. You will collaborate cross-functionally with R&D, Quality, and Clinical teams to ensure...

## Regulatory Affairs SpecialistApplyremote type:Not Remotelocations:Polinyà, Spain:MERU CEDEX, France:Gdansk, Poland:Poland:Pinneberg, Germanytime type:Full timeposted on:Posted 2 Days Agotime left to apply:End Date: July 29, 2026 (18 days left to apply)job requisition id:JR8439**You Speak Up to Share Opportunities for Improvement and Drive Change? Would...