Manager, RA Submissions

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 Product Submissions and Registration

Job Category:
Professional

All Job Posting Locations:
High Wycombe, Buckinghamshire, United Kingdom

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.

Learn more at https://www.jnj.com/innovative-medicine

We are searching for the best talent for a Manager, RA Submissions.

This hybrid work position will be located in High Wycombe, United Kingdom

We are pleased to announce that from mid-2026, our offices in Wokingham and High Wycombe will move into a modern, state-of-the-art Johnson & Johnson office in central Maidenhead, conveniently situated next to the train station.

The Manager, RA Submissions is a highly independent position, responsible for the submission operational management and delivery of global regulatory submissions required at a compound level to support the development, registration, and compliance of products.  This position works under minimal direction and is responsible for organizing their own time efficiently to maximize contributions.

Key Responsibilities:


* Coordinate the preparation and maintenance of global regulatory submissions and filings in line with regulatory strategy.


* Create and manage dossier plans/submission packages, seeking input from regulatory therapeutic areas, functional area representatives, and key partners, while providing guidance to project team members.


* Contribute to decisions that have an impact on the quality and timeliness of Health Authority submissions.


* Make decisions on submission operational strategies for an optimal project management approach within process/timeline/resource constraints.


* Lead cross-functional submission team meetings to coordinate the preparation and maintenance of regulatory submissions and filings.


* Leadership role for the monitoring and efficiency of the submission process, initiate changes within the scope of decision-making authority to optimize efficiencies and ensure quality.


* Cultivate effective relationships, maintaining open commun...