Regeneron UK Limited Posted August 28, 2026

Senior Manager GD GCP Auditing (UK)

Remote, United Kingdom Full time
Quality Manager
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Regeneron UK Limited is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

Build our future together:

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager GD GCP Auditing to join our Global Development Quality Assurance team, supporting our global development organization in a remote work model. In this role, you will lead risk-based quality auditing activities and strengthen GCP compliance while collaborating with Global Development teams, external partners, and quality stakeholders. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.

When & where:

Location: United Kingdom

Work model: Remote

Discover your role:

Lead end-to-end GCP audits across internal and external global activities.

Schedule, conduct, report, and follow up on routine and directed audits.

Develop and execute risk-based audit programs for assigned clinical studies.

Identify compliance issues and drive process improvements and standardization.

Representing Quality Assurance on complex compliance projects and initiatives.

Interpret policies, standards, and regulations to address critical issues.

Support regulatory inspections and inspection room activities.

You thrive in a dynamic environment and build trusted stakeholder partnerships.

This role requires:

Bachelor’s degree with 8+ years of relevant industry experience; Master’s degree preferred.

At least 5 years of direct Good Clinical Practice audit experience.

Expert knowledge of FDA regulations, European Union regulations, ICH guidance, and GCP requirements.

Experience conducting audit types including process, site, vendor, and partner audits.

Experience with regulatory inspections involving investigator sites, sponsors, or Contract Research Organizations.

Ability to independently manage complex GxP compliance issues and high-value priorities.

Strong leadership skills with experience interfacing with senior leaders.

Excellent project management, stakeholder management, collaboration, and negotiation skills.

Strong problem-solving, written, and verbal communication skills.

Ability to work independently, take initiative, and perform effectively in ambiguous environments.

High attention to detail, accuracy, and organizational awareness.

Willingness to travel 30-40% domestically and internationally.

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/ . 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.

Job details

Seniority
Manager
Function
Quality
Therapeutic area
Not listed
Location
Remote, United Kingdom
Employment type
Full time

How this role compares

Computed from every other active Quality role in our database, not just this employer's listings.

We currently track 246 comparable Manager Quality roles across 80 biopharma companies.

246Comparable roles tracked
230Currently active
80Companies hiring similar roles
33Countries represented

Salary context

59 of 246 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · Quality Control Associate Scientist- Overnight Shift · Merck KGaA $27/hr – $46/hr (≈ $56,160–$95,680/yr)
Peer group range $75,920 – $208,845 (median $175,750)

Where these roles are based

Top locations among the 246 comparable roles

United States88
China27
India16
Ireland16
Japan12
China's Mainland7

+ 27 more countries

Seniority mix

246 of 246 peers have a known seniority level

Manager181
Associate Director42
Associate23

Therapeutic area mix

1 of 246 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Rare Disease1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

60%similar
Remote, United Kingdom Manager
Same function Same seniority Same country
60%similar
Regeneron UK Limited Remote, United Kingdom Manager
Same function Same seniority Same country
60%similar
Ipsen Biopharm Ltd London (UK), United Kingdom Manager
Same function Same seniority Same country
60%similar
Sandoz Cambridge (United Kingdom), United Kingdom Manager
Same function Same seniority Same country
50%similar
Roche Welwyn, Hertfordshire, United Kingdom Associate
Same function Adjacent seniority Same country
50%similar
Johnson & Johnson High Wycombe, United Kingdom Associate Director
Same function Adjacent seniority Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

60%
Senior Manager QA Auditor GCP Strategy
· Remote, United Kingdom · Manager
Function Therapeutic area Seniority Country
60%
R&D Quality Manager
Sandoz · Cambridge (United Kingdom), United Kingdom · Manager
Function Therapeutic area Seniority Country
45%
Senior Manager, Clinical Quality Assurance
AbbVie · North Chicago, IL · Manager
Function Therapeutic area Seniority Country
45%
Senior Manager, Quality Assurance (GMP Operations)
Gilead Sciences, Inc. · Foster City, United States · Manager
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.