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
You will lead the MSAT Technical Execution team in the United States. You will coach and develop a team that supports product and process performance across the manufacturing lifecycle. You will work closely with manufacturing, quality, engineering and supply chain to solve problems, enable changes, and drive continuous improvement. We value a hands-on leader who brings technical credibility, practical problem solving, and a focus on people development. This role offers visible impact, strong career growth, and the chance to help GSK unite science, technology and talent to get ahead of disease together.

Responsibilities
This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:

• Lead and develop a multidisciplinary MSAT Technical Execution team to deliver reliable day-to-day technical support.
• Own technical readiness for product changes, transfers, upgrades and process improvements.
• Provide expert support for investigations and root cause analysis for complex process and equipment issues.
• Ensure technical deliverables meet quality, regulatory and safety expectations through clear documentation and handover.
• Use data and metrics to track product and process performance and drive continuous improvement.
• Collaborate with operations, engineering, quality and supply chain to prioritize work and resolve issues quickly.

Why You?

Basic Qualification
We are seeking professionals with the following required skills and qualifications to help us achieve our goals:

• Bachelor’s degree in engineering, life sciences or related technical field.
• 8+ years of experience in pharmaceutical or biopharmaceutical manufacturing or MSAT roles.
• Experience with process troubleshooting, investigations and technical change execution.
• Experience leading small to medium technical teams or project groups.

Preferred Qualification
If you have the following characteristics, it would be a plus:

• Advanced degree in engineering, biotechnology or related field.
• Experience with technical transfer, scale-up and process validation.
• Familiarity with aseptic processing, sterile drug product operations or biologics manufacturing.
• Strong data analysis skills and experience with tools for trending and root cause analysis.
• Proven ability to lead cross-functional change and deliver projects on time.
• Experience working in a hybrid environment and supporting 24/7 operations.
• Ability to communicate clearly with technical and non-technical stakeholders.
• Demonstrated knowledge of Good Manufacturing Practice (GMP) requirements and regulated environments.

Working model
This role will be onsite or hybrid depending on site needs. The hiring team will confirm the specific working model during the recruitment process.

What we value in you
We want you to bring practical technical leadership, clear communication and a coaching mindset. You should enjoy solving problems with others and be committed to safe, compliant and effective manufacturing. We welcome people who value inclusion and who will help build an open and supportive team culture.

Ready to apply?
If you are motivated to help improve product and process performance and to develop people, we want to hear from you. Apply now to join a team that delivers solutions that matter to patients and communities.

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Please visit  GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees.

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.

If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at - [email protected]

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.

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