Senior Audit Lead (EMEA GMP Audit)

Are you an experienced Biopharm, Vaccines, or Pharmaceutical professional looking for an exciting opportunity to leverage your expertise to support GSK Senior Management in the identification, prioritisation, and monitoring of quality, compliance, and technical risks? If so, this role within our Quality organisation could be a great opportunity for you.

Position Details:

The purpose of the Audit Senior Lead role is to perform and manage GMP (Good Manufacturing Practice) and Compliance audits of Steriles, Biopharm, Vaccines, and Pharmaceutical facilities that supply highly regulated markets. You will be responsible for evaluating the compliance of GSK Global Supply Chain (internal and external) facilities with GMP, applicable policies and procedures, and regulatory and contractual commitments. Your remit will include audits of (Global Supply chain internal and external networks) manufacturing facilities and operations, Local Operating Companies (LOCs), R&D and Logistics Service Providers (LSPs).

In this role, you will also provide sterile manufacturing subject matter expertise for the GSK Global Supply Chain EMEA auditing team.

Please Note:  Strong knowledge / experience of sterile, vaccines and / or biopharm manufacturing processes (alongside communication and influencing skills) are considered essential for delivering in this role.

Key Responsibilities include:

More experienced staff may undertake:

Manage complex stakeholder engagement for audits across the network (which may include Supply Chain Directors, Site Directors, Site Quality Directors, VPs/Heads of support functions, and Research & Development Quality).

Typical work output will involve:

Performing audits of Global Supply Chain (GSC) sites, LOCs, and external manufacturing sites (including R&D), LSPs and facilities supplying EMEA and other highly regulated markets.

Preforming Unannounced audits.

Preforming for-cause audits based on regulatory actions or identified risk.

Preforming process, quality system-specific, and targeted audits.

Performing audits against risk mitigation plans or regulatory citation commitments.

As an output, it is critical to produce clear, concise, and accurate audit reports to ensure senior management is appraised of identified risks and that appropriate corrective action plans are implemented.

Location:  This role can be based at any of the following manufacturing sites:  Ware, Worthing, Barnard Castle (UK), Wavre, Rixensart (Belgium), St Amand (France), or Tres Cantos (Spain).

Travel: Please note that the successful applicant will need to travel to sites across the network as part of the role. We anticipate travel will be approximately up to 40% of your time.

CLOSING DATE for applications: Monday 24th of August 2026 (COB).

Basic Qualifications:

We are looking for professionals with the following required skills:

Degree in a relevant Scientific, Technical or Engineering discipline.

Relevant and specific experience obtained from working in Steriles, Biopharm &/or Vaccines.

Subject matter expertise / knowledge of world-wide cGMPs, regulatory requirements, standards and Quality Management Systems for Steriles/ Biopharm / Vaccines / Pharmaceutical Manufacturing and Packing.

Experience in identifying and/or managing complex Quality and Compliance risks and issues.

Preferred Qualifications:

If you have the following skills and characteristics, it would be a benefit:

Previous auditing experience preferred (e.g. Proficiency and experience in planning, performing and reporting Quality and Regulatory Compliance audits).

Working knowledge and ability in evaluation of Data Integrity and ALCOA+ principles within the Pharmaceutical industry.

Increasing knowledge of AI tools, applications and ways of working in the Pharmaceutical industry

Auditor formal accreditation/certification.

Experience managing the interface with stakeholders (Site Directors, Site Quality Directors, VPs and Heads of Support Functions).

If you would like to learn more about our company wide benefits and life at GSK we would suggest looking at our webpage Life at GSK | GSK .

Skills

Data Integrity, Digital Fluency, GxP Regulations, Influencing Without Authority, Lean Management, Pharmaceutical Regulatory Compliance, Problem Solving, Quality Assurance (QA), Quality Auditing, Risk Awareness, Technical Writing

French Salary Range / Fourchette salariale – France EUR 78,750 to EUR 131,250Spanish Salary Range / Rango salarial en España: EUR 66,150 to EUR 110,250Belgium Salary Range / Fourchette salariale – Belgique: EUR 78,750 to EUR 131,250The annual gross base salary range for new hires in this position is listed above for each applicable location. These ranges take into account a number of factors including the candidate’s skills, experience, education level and the market rate for the role. In addition, this position may offer an annual bonus and eligibility to participate in our share based long term incentive program which is dependent on the level of the role. More detailed information on the total benefits package will be supplied during the recruitment process. This role is available for applicants from multiple locations, and therefore salary ranges for certain locations are also shown. Salary ranges for other locations are shown because some markets have pay transparency laws that require salary information on job postings, and those locations are potential job sites for this role. If salary ranges are not displayed in the job posting for a specific location or country, the relevant compensation will be discussed during the recruitment process. Please note salaries vary by country based on the candidate’s skills, experience, education level and the market rate for the role. Offers are typically made within the advertised range based on the candidate’s skills, experience and qualifications, with the upper end generally reserved for highly experienced candidates or other exceptional circumstances aligned with these criteria.

Why GSK?

Uniting science, technology and talent to get ahead of disease together.

GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.

People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.

GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.

We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are.

Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us at UKRecruitment.Adjustments@gsk.com where you can also request a call.

Please note should your enquiry not relate to adjustments, we will not be able to support you through these channels. However, we have created a  Recruitment FAQ guide. Click the link where you will find answers to multiple questions we receive

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