OQ Team Lead (Quality Oversight)
GSK
Zebulon, North Carolina
Full-Time
Competitive
HybridManager
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 a small Operational Quality team that provides quality oversight across manufacturing. You will work closely with manufacturing, and supply chain colleagues to protect product quality and patient safety. We value clear decision-makers who simplify processes, coach others, and drive measurable improvement. This role offers visible impact, career growth and the chance to unite science, technology and talent to get ahead of disease together.
Responsibilities:
Lead and coach the Operational Quality team to deliver consistentoversightof the Quality Management System. Monitor quality performance using metrics and trends, escalate risk, andcollaborateoncorrectiveaction plans.
Oversee investigations of deviations, non-conformances and complaint-related issues and drive robust root cause analysis. Review and approve batch records,certificatesand quality documentation to meet regulatory and good documentation standards.
Support product introductions, transfers and changes,prepare for and support audits and inspections,and coach internal teams and external partners on inspection readiness.
Provide oversight, support,andaccuratescheduling of activities to the quality team responsible for quality oversight of all GMP areas ensuring all requirements have been met, and the defined schedule is followed.
Maintain presence acrossareasof responsibility and be the first line of contact to support initial management of quality issues and be accountable for key quality decision making across activities such as theinitialimpact assessment for deviations.
Provide guidance during GMP activities to proactively detect potential quality issues through active observation in real-time, allowing fortimelyinterventions to prevent deviations and defects
Perform a spot-check of activities across defined GMP areas to ensure compliance with quality standards thatincludeproduction, testing,QC,warehouse,facilitiesandutilities.
Collaborate with cross-functional teams to resolve quality issues, implement corrective/preventive actions (CAPAs) and support continuous improvement efforts.
Review GMP documentation and records ensuring Good Documentation Practice (GDP) is beingmaintainedfollowing ALCOA++ principles for data integrity,auditand traceability
Check that facilities are beingmaintainedin a good state in line with local housekeeping standards and any deviation from the standards are escalated and supporttimelyimplementation of remedial actions
Track and trend quality oversight observations on collected data andfacilitatemitigation actions and regularly update andmaintainthe quality oversight risk assessment
Participates in and supports site-based audits/inspections as SME for Quality Oversight.
Basic Qualifications:
We are seeking professionals with the following required skills and qualifications to help us achieve our goals:
Bachelor’s degree in science, pharmacy, engineering, or a related discipline, or equivalent experience.
6+ years of manufacturing experience from pharmaceutical industry, biologics manufacturing, distribution, supplier quality, or quality operations.
Experience with quality systems such as deviations, CAPA, change control, and document control.
Experience with data trending, statistical analysis, and root cause analysis tools.
Experience across multiple dosage forms,packagingor device assembly activities.
Proven experience and strong knowledge of the application of the principles of Quality Management Systems (QMS)
Strong written and verbal communication skills for cross-functional collaboration and supplier engagement
Preferred Qualifications:
If you have the following characteristics, it would be a plus:
Leading or supervising a quality team in operations or supplier quality. Working knowledge of Good Manufacturing Practices and applicable U.S. regulatory expectations.
Familiarity with inspection readiness and supporting regulatory inspection responses.
Work model:
This role is an onsite position which requires you to be onsite. This is not a hybrid position.
What we value:
We act with transparency, respect and integrity. We make evidence-based decisions and balance speed, rigor and risk. We welcome applicants from all backgrounds and support an environment of inclusion where everyone can do their best work.
Ready to apply?
If you are motivated to lead operational quality, protect patients and improve systems, please apply. Tell us how your leadership and quality experience will help our team succeed. We look forward to hearing from you.
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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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