Johnson & Johnson Regulatory Affairs Job – Apply Now!
Join Johnson & Johnson, a global leader in healthcare innovation, as an Experienced Regulatory Affairs Professional. This role supports the development and registration of Haematology and Solid Tumor Oncology products across Europe, the Middle East, and Africa (EMEA). Be part of a patient-focused team that pioneers medical breakthroughs and shapes regulatory strategies. Apply now to contribute to cutting-edge healthcare advancements.
About the Company
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow and profoundly impact health for humanity.
- Job Posting: Experienced Professional Regulatory Affairs
- Company: Johnson & Johnson
- Location: Leiden, South Holland, Netherlands
- Job Function: Regulatory Affairs
- Job Locations:
Beerse, Antwerp, Belgium, Issy-les-Moulineaux, Hauts-de-Seine, France, Leiden, South Holland, Netherlands, Madrid, Spain, Warsaw, Masovian, Poland
Job Description
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
Job Details
Janssen EMEA Oncology is recruiting for a dedicated Experienced or Senior Regulatory Affairs Professional to work on the development and registration of Haematology or Solid Tumor Oncology products in Europe, the Middle East, and Africa (EMEA). The position can be based in Belgium, The Netherlands, or the United Kingdom. The job provides an opportunity to support small and large molecules, as well as advanced therapies, and various oncology indications, contributing to healthcare one patient at a time.
Responsibilities
- Input in clinical development and post-approval
- Liaison with Regulatory Agencies and Local Operating Companies
- Input in document and process development
- Clinical Trial Applications
- Marketing Authorization Applications
Job Requirements
Education and Experience
- Master’s degree – medical or paramedical (pharmacy, biology, veterinary, etc.), or equivalent by experience
- 2+ years of experience in regulatory affairs (4+ years for Senior positions)
Skills
- Project management
- Strong oral & written communication skills
- Organization and multitasking skills
Knowledge
Knowledge of medicines regulatory environment in EMEA, particularly the EU
Note: This role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements.
If you are interested, please apply through the specific requisition number for your preferred location:
- United Kingdom – Requisition Number: R-005901
Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.
Keywords: Johnson & Johnson, Experienced Professional, Regulatory Affairs, Healthcare, Innovative Medicine, Oncology, EMEA
