Business IntroductionWe 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 SummaryThe Quality Control Director is responsible for leading Quality Control laboratory operations to ensure they are organizationally, technically, and operationally prepared to support commercial manufacturing and new product introductions across the validation lifecycle.
This role provides scientific and operational leadership across analytical, biochemical, and microbiological laboratories supporting raw material testing, in-process and finished product testing, and stability programs. The position partners cross-functionally to ensure inspection readiness, regulatory compliance, and reliable delivery of high-quality laboratory data that supports site objectives and regulatory commitments.
ResponsibilitiesThis role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:
- Lead and oversee Quality Control laboratory operations supporting GMP testing, release, and stability programs.
- Ensure laboratories are inspection-ready and operate in compliance with regulatory and quality system requirements.
- Provide leadership for QC readiness activities related to new product introductions, technology transfers, and lifecycle changes.
- Oversee method transfer and assay qualification activities in alignment with technical and regulatory requirements.
- Ensure effective QC organizational readiness, including staffing, training, onboarding, and capability development.
- Support QC involvement in commissioning, qualification, and validation activities for laboratory facilities, equipment, and systems.
- Ensure laboratory data integrity, documentation accuracy, and adherence to ALCOA principles.
- Partner with Manufacturing, QA, Engineering, Validation, and Development to support site priorities.
- Support internal and external audits and regulatory inspections.
- Contribute to continuous improvement initiatives and operational excellence within the QC organization.
Why You?Basic QualificationWe are seeking professionals with the following required skills and qualifications to help us achieve our goals:
- Bachelor's degree in a scientific or technical discipline (e.g., Chemistry, Biochemistry, Microbiology, or related field).
- Minimum of 8 years of supervisory/managerial experience within a regulated GMP environment.
- Demonstrated experience in Quality Control laboratory operations.
- Experience supporting regulatory inspections and audits.
- Working knowledge of quality systems and regulatory expectations.
- Demonstrated ability to lead teams and work cross-functionally to manage priorities and deliver results.
Preferred QualificationIf you have the following characteristics, it would be a plus:
- Master's degree or PhD in a scientific discipline.
- Experience supporting new product introductions, method transfers, or technology implementations.
- Experience with digital laboratory systems, automation, or data/reporting tools.
Work ArrangementThis role is on-site or hybrid, depending on site requirements. Remote-only working is not available.
How to ApplyIf you are motivated to lead a lab team, improve processes, and help deliver high quality supply for patients, we want to hear from you. Please submit your application and tell us how your experience and leadership would support our goals. We welcome applicants from all backgrounds and encourage people who will bring new perspectives to apply.
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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.
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[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.
Important notice to Employment businesses/ AgenciesGSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.
Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/
