[Skip to main content](#main-content)

[ OpenNash ](https://opennash.com/) / [Jobs](https://jobs.opennash.com/) [ 01 Search jobs](https://jobs.opennash.com/search/)[ 02 Companies](https://jobs.opennash.com/explore/)[ 03 Hiring report](https://jobs.opennash.com/reports/hiring/)[ 04 AI assistants](https://jobs.opennash.com/connect/)[ 05 How it works](https://jobs.opennash.com/methodology/)

Regeneron Pharmaceuticals · Uxbridge

# Associate Manager Regulatory Affairs

Uxbridge Hybrid Manager or lead Legal & Compliance 

Listed on Regeneron Pharmaceuticals’s official careers site. Posted October 20, 2026. Check that it is still open and apply there.
[Apply on Regeneron Pharmaceuticals’s careers site →](https://careers.regeneron.com/en/jobs/r51785/associate-manager-regulatory-affairs/)

[OpenNash Jobs](https://jobs.opennash.com/) / [Regeneron Pharmaceuticals](https://jobs.opennash.com/companies/regeneron-pharmaceuticals/) / Associate Manager Regulatory Affairs

## Job description

### Build our future together

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Manager, Regulatory Affairs to join our UK regional team, supporting our UK and Ireland markets in a hybrid setting. In this role, you will support marketing authorisations and licence maintenance across therapeutic areas while collaborating with local, regional and global colleagues.

This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.

### When & where

Uxbridge (Hybrid)

### Discover your role
- Prepare, compile and lead timely marketing applications and post-approval variations through Medicines and Healthcare products Regulatory Agency (MHRA) pathways.
- Support submission strategies, negotiate with MHRA partners and communicate implementation to UK and Ireland teams.
- Author, review and manage module documents, responses and UK Paediatric Investigational Plans alongside pre-submission and scientific advice meetings.
- Support UK labelling, artwork and related meetings alongside UK/Ireland promotional and additional risk minimisation material reviews.
- Represent regulatory across commercial, medical, patient safety, quality and global submissions teams within the European Union (EU) regional team.
- Maintain local regulatory knowledge and UK/Ireland compliance while supporting UK and EU clinical trial applications and inspections.
- Develop best-practice user guides, work instructions and standard operating procedures through departmental initiatives.
- You bring a proactive, collaborative approach to regulatory challenges.

### This role requires
- Bachelor’s or advanced degree in life sciences, pharmacy or a related scientific field.
- UK/Ireland regulatory experience, approximately up to two years, managing Type II clinical variations and approvals through MHRA pathways.
- Experience handling post-Brexit UK applications and regulatory pathways.
- Knowledge of clinical trial requirements, procedures and EU medicines development.
- Regulatory database proficiency and ability to manage parallel submissions against firm deadlines and changing priorities.
- Strategic thinking, commercial awareness, excellent written/verbal communication and ability to foster strong global matrix teamwork.
- UK rare disease therapeutic-area experience preferred.

Does this sound like you?

Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law.

Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits.

For additional information about Regeneron benefits in the U.S., please visit [https://careers.regeneron.com/en/working-at-regeneron/total-rewards/](https://careers.regeneron.com/en/working-at-regeneron/total-rewards/). For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter.

Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.

As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.

### For jobs in Canada

this posting is for an existing position.

## At a glance
- Posted by the employer: Oct 20, 2026
- First seen by OpenNash: Oct 26, 2026
- Last checked: Nov 2, 2026
- Listed for: 13 days
- Location: Uxbridge
- Work arrangement: Hybrid[Apply on Regeneron Pharmaceuticals’s careers site →](https://careers.regeneron.com/en/jobs/r51785/associate-manager-regulatory-affairs/)

## Hiring at Regeneron Pharmaceuticals
- Open jobs: 866
- New in the last 7 days: After two weekly collections
- Tracked since: Jul 15, 2026

[All Regeneron Pharmaceuticals jobs](https://jobs.opennash.com/companies/regeneron-pharmaceuticals/) · [Weekly hiring report](/reports/hiring/)

## More jobs at Regeneron Pharmaceuticals

### [Associate Director Global Patient Safety](https://jobs.opennash.com/companies/regeneron-pharmaceuticals/jobs/741eb97063ea911534dd/)

Uxbridge

### [Associate Director Medical Affairs UK (Oncology)](https://jobs.opennash.com/companies/regeneron-pharmaceuticals/jobs/363c6233a8a882872919/)

Uxbridge

### [Associate Director, Global Patient Safety Standards & Training](https://jobs.opennash.com/companies/regeneron-pharmaceuticals/jobs/02719b06989beff32449/)

Uxbridge

### [Associate Director, Precision Medicine (Clinical Diagnostics)](https://jobs.opennash.com/companies/regeneron-pharmaceuticals/jobs/22483f0c323aabfd5b8c/)

Uxbridge

### [Director International Commercialization Immunology](https://jobs.opennash.com/companies/regeneron-pharmaceuticals/jobs/65a2a5e020da2a68c6cc/)

Uxbridge

## Similar jobs at other companies

### [Regulatory Affairs Manager, Oncology Therapeutic Group, Global Regulatory Affairs](https://jobs.opennash.com/companies/gsk/jobs/09fdd8d7e12226e3ad65/)

GSK · London, United Kingdom

### [Senior Regulatory Specialist I - Toxicology, Global Regulatory Affairs](https://jobs.opennash.com/companies/ecolab/jobs/a7f265c77c592a38c347/)

Ecolab · Pune, Mahārāshtra, India

### [Regulatory Affairs Specialist](https://jobs.opennash.com/companies/ecolab/jobs/2f207cd244cb549328ab/)

Ecolab · Kraków, Poland

### [Principal Regulatory Affairs Professional](https://jobs.opennash.com/companies/thermo-fisher-scientific/jobs/3a8ef8a0559f4968a312/)

Thermo Fisher Scientific · Remote, Mexico

### [Regulatory Affairs Specialist](https://jobs.opennash.com/companies/thermo-fisher-scientific/jobs/c80907ca1d5f566fcec5/)

Thermo Fisher Scientific · Bangalore, Karnātaka, India

OpenNash lists jobs from employers’ own careers sites and does not handle applications.
Dates come from the employer where stated; “first seen” and “last checked” are our own observations.

[ OpenNash ](https://opennash.com/)

AI-native services firm that builds custom software and 24/7 AI agents.

OpenNash Jobs is an OpenNash Applied AI project.
[Book time with OpenNash](https://calendly.com/opennash/new-meeting?hide_gdpr_banner=1)

Jobs
- [Search jobs](https://jobs.opennash.com/search/)
- [Companies](https://jobs.opennash.com/explore/)
- [Hiring report](https://jobs.opennash.com/reports/hiring/)
- [AI assistants](https://jobs.opennash.com/connect/)
- [How it works](https://jobs.opennash.com/methodology/)

OpenNash
- [opennash.com](https://opennash.com/)
- [Services](https://opennash.com/ai-agent-consulting/)
- [OpenNash CX](https://opennash.com/cx/)
- [AI Tools](https://opennash.com/ai-tools/)
- [Blog](https://opennash.com/blog/)
- [About](https://opennash.com/about/)

Contact
- [hello@opennash.com](mailto:hello@opennash.com)

- [LinkedIn](https://www.linkedin.com/company/opennash)

- [Support](https://jobs.opennash.com/support/)

- [Privacy](https://jobs.opennash.com/privacy/)

- [Terms](https://jobs.opennash.com/terms/)

© 2026 OpenNash, Inc. Company names and public job postings belong to their respective owners. Employers control source availability and application decisions.
