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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
The Senior QA Documentation Specialist is responsible for advanced oversight, governance, and continuous improvement of cGMP quality systems supporting vaccine manufacturing at the Marietta site. This role serves as a recognized subject matter expert (SME) for Documentation systems, with increased accountability for system performance, regulatory compliance, inspection readiness, and data integrity.
The Senior QA Documentation Systems Specialist provides evaluates quality risks, leads complex investigations and CAPAs, provides quality decision‑making for their assigned system. The individual partners cross‑functionally to ensure quality systems are robust, effective, and aligned with global and regulatory expectations.
Responsibilities
This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:
Why You?
Work model
This role is hybrid. You will be on site regularly and will have flexibility to work remotely. Occasional travel to supplier sites and audits is expected.
Basic Qualification
We are seeking professionals with the following required skills and qualifications to help us achieve our goals:
Preferred Qualification
If you have the following characteristics, it would be a plus:
Master’s degree in science or business discipline or an additional BS.
Strong ability to influence cross-functional stakeholders and drive compliance without direct authority
What we value
We act with transparency, respect and integrity. We make evidence-based decisions and balance speed, rigor and risk. We welcome people from all backgrounds and support an environment of inclusion where everyone can do their best work. We value those who are curious, collaborative and committed to improving quality for patients.
Ready to apply?
If you are passionate about clear, compliant documentation and want to make a meaningful impact, please apply. Tell us how your skills in documentation and quality will help our team and our mission to get ahead of disease together. We look forward to hearing from you.
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Skills
Data Integrity, Detail-Oriented, Digital Fluency, GxP Regulations, Influencing Without Authority, Lean Management, Pharmaceutical Regulatory Compliance, Problem Solving, Quality Assurance (QA), Risk Awareness, Technical Writing
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 - usrecruitment.adjustments@gsk.com
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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