EQ Small Molecules Senior Lead - TPS in London

Closing Date: 6th February 2026 (COB)

Business Introduction

We manufacture and supply reliable, high-quality medicines and vaccines to meet patients' needs and drive our performance. Our network of 37 medicines and vaccines manufacturing sites delivered 1.7 billion packs of medicines and 409 million vaccine doses in 2024 to help make a positive impact on the health of millions of people. Our supply chain is not just core to our operations; it's vital to bringing our innovations to patients as quickly, efficiently and effectively as possible. Technology is transforming how we manufacture medicines and vaccines, enabling us to increase the speed, quality and scale of product supply. We need the very best minds and capability to help us on our journey to make more complex products, harnessing the power of smart manufacturing technologies including robotics, digital solutions and artificial intelligence to deliver for patients.

Position Summary

We are seeking an experienced and strategic External Quality Senior Lead (TPS Quality Lead) to drive the quality partnership and ways of working across external manufacturing partners (Third Parties) and internal GSK functions. This role is central to ensuring high standards of product quality, regulatory compliance, and consistent execution across our external supply network.

Responsibilities

• Provide strategic leadership to drive a high-performing partnership model between External Quality, Third party and global GSK functions, ensuring aligned priorities, proactive risk management and robust governance.
• Lead and influence Quality Agreement negotiations with Third Parties, shaping contractual frameworks and ensuring global compliance and operational excellence across the network.
• Drive relationships with Third party, GSK internal sites by strong governance and contractual performance management to strengthen quality and supply resilience.
• Act as the senior quality decision-maker for business-critical evaluations and change processes, ensuring alignment with regulatory expectations, QMS standards and long-term business objectives.
• Direct the resolution of escalated quality issues and cross‐site quality programmes, guiding root cause investigations, CAPA effectiveness and continuous improvement to comply with global quality performance.
• Serve as a senior Quality SME influencing partnerships and lifecycle strategies, while coaching internal and external leaders to embed a culture of compliance, accountability and operational excellence.

Working Pattern

The role can be based in the United Kingdom or France and follows a hybrid working model of at least 2 days per week in the office.

Basic Qualification

• Significant experience in pharmaceutical/biopharmaceutical quality roles with direct exposure to supplier/CMO management.
• Qualified Person (QP) designation is required.
• Strong understanding of Quality Systems, GMP, regulatory requirements and how they apply to external manufacturing.
• Proven experience negotiating Quality Agreements and establishing supplier quality KPIs and performance frameworks.
• Experience working closely with Legal and Business Partners on contractual and commercial matters.
• Exceptional written and verbal communication skills in English (high level); comfortable interacting with global teams and external suppliers.

Preferred Qualification

• Experience in biologics/complex modalities.
• Previous experience in a multinational pharma company or working across multiple regions/LOCs.
• Project management or change management qualification.
• Experience liaising with co-owners of shared brands and managing cross-company PIRC interactions.

What we offer

• The opportunity to shape the supplier quality strategy for a leading pharmaceutical organization.
• Collaborative, diverse and supportive working environment.
• Competitive salary and benefits package.
• Career development and professional growth opportunities.

How to apply

If this role feels like a good next step, please apply now. Tell us how your experience will help deliver safe, compliant outcomes and drive successful integrations or transfers. We look forward to hearing from you.

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.