Job Description

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. Learn more at https://www.jnj.com

Job Function:

Regulatory Affairs Group

Job Sub Function:

Regulatory Affairs

Job Category:

Professional

All Job Posting Locations:

High Wycombe, Buckinghamshire, United Kingdom

:

About Johnson & Johnson

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. Learn more at https://www.jnj.com/.

Janssen EMEA Neuroscience, Cardiovascular, Metabolic and Retina (NCMR) team is recruiting for a dedicated Experienced Regulatory Affairs Professional to work on the development and registration of NCMR products in Europe, the Middle East, and Africa (EMEA). The job provides an opportunity to support small and large molecules, as well as advanced therapies, and in different NCMR disease areas, contributing to healthcare one patient at a time.


This role is preferred to be located in one of our J&J EMEA hubs (Beerse, Belgium; High Wycombe, UK; Leiden, the Netherlands; Madrid, Spain or Warsaw, Poland)


Please note that this role is available across multiple countries and may be posted under different requisition numbers to follow local requirements. While you are welcome to apply to any or all of the postings, we recommend focusing on the specific country(s) that align with your preferred location(s).


Beerse, Leiden, Madrid, Warsaw - Requisition Number: R-053480


Remember, whether you apply to one or all of these requisition numbers, your applications will be considered as a single submission.

Please note that our office will be relocating to central Maidenhead from October 2026. Applicants should ensure that this location is suitable for them.


The successful applicant will help develop and implement regulatory strategies to achieve efficient development and timely commercialization of innovative pharmaceutical products in compliance with applicable regulations.

1. Input in clinical development and post-approval

Support the EMEA Regulatory Liaison in developing the regulatory strategy for products in development and assist in submissions to health authorities from early development, CTAs to MAAs and life-cycle management. Contribute to Global Regulatory Team meetings as the EMEA Regulatory Professional Guide project teams on applicable regulatory requirements, contribute to regional and local regulatory strategy, and help address project-specific regulatory issues Develop an understanding of the regional regulatory environment, competitor intelligence, and therapeutic areas

2. Liaison with Regulatory Agencies and Local Operating Companies

Act as backup for contact with EMA and national Regulatory Agencies Support the preparation of meetings with Regulatory Agencies Collaborate with LOCs, track and respond to queries in a timely manner

3. Input in document and process development

Assist in the creation and revision of processes related to regulatory submissions Draft and review document content based on regulatory knowledge Contribute to and support the development of briefing documents, paediatric investigational plans, orphan drug designations, and response documents, where required Provide input to response documents to ensure they thoroughly and accurately answer the questions being posed Track dates of regulatory agency submissions, questions, responses, and approvals

4. Clinical Trial Applications

Review protocols and ensure alignment with regulatory requirements Provide guidance to team on CTA submission strategies and documents Ensure CTA submission packages are complete according to agreed timelines

5. Marketing Authorization Applications

Provide regulatory support throughout the life-cycle of a product. Guide and collaborate with cross-functional teams on required documents and submission strategies in preparation for MAA Identify and supervise critical path activities Assist with timely submission and acceptance of MAA Ensure country-specific submission packages are made available to the local operating companies (LOCs) in accordance with agreed plans

Job Requirements

Education and experience

Bachelor's degree in Life Sciences, Pharmacy, or a related field; advanced degree

preferred, or equivalent by experience

Proven experience of 2+ years in regulatory affairs or other relevant functions. Experience working in cross-functional teams

Skills

Project management Strong oral & written communication skills Organization, prioritising, and multi-tasking skills

Knowledge

Knowledge of the pharmaceutical regulatory environment, guidelines, and practice in EMEA, particularly the EU.

Required Skills:

Preferred Skills: