Product & Process Compliance Specialist

Responsibilities

• Serve as the primary quality contact for assigned areas during production and project activities.
• Evaluate risk and quality impact for proposed changes and support cross-functional risk assessments.
• Prepare clear, inspection-ready change records, deviation reports, and investigation summaries.
• Track and trend quality KPIs and provide inputs for site quality meetings.
• Support internal audits and prepare summary reports, act as a subject matter contributor during external inspections.
• Ensure quality obligations with third-party providers are managed and resolved promptly.
• Why You?
• Basic Qualification
• We are seeking professionals with the following required skills and qualifications to help us achieve our goals:
• Associate degree in a science, engineering, quality, or related field, or equivalent experience.
• Minimum 1+ year experience in a regulated life science, pharmaceutical, or biotech quality role.
• Practical knowledge of Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP).
• Experience with quality systems such as change control, deviations, CAPA, or document management.
• Preferred Qualification
• If you have the following characteristics, it would be a plus:
• Bachelor's degree in a scientific, engineering, or quality discipline.
• Experience in biologics or pharmaceutical manufacturing, laboratory operations, or secondary packaging.
• Experience with electronic quality systems or document management tools (for example, Veeva Vault or similar).
• Formal training in root cause analysis methodologies (for example, DMAIC, 8D).
• Strong interpersonal skills and ability to work well across functions and levels.
• Experience supporting validation, qualification, or Process Performance Qualification activities.
• Demonstrated ability to perform root cause analysis and author investigation reports.
• Strong attention to detail and ability to follow written procedures and deadlines.
• #LI-GSK
• #GSKMarietta
• #MariettaGSC
• Work Arrangement
• This role is on-site. You will be required to be present at the site to provide hands-on quality support and shop-floor engagement.
• How to apply
• Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees.
• Why

Benefits

Additional Information

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 support product and process compliance activities across a manufacturing site in the United States. You will work closely with operations, engineering, laboratory, regulatory, and quality colleagues. You will help manage change control, investigate deviations, and keep quality systems inspection-ready. We value practical problem solving, clear communication, and a commitment to patient safety. This role offers hands-on experience, cross-functional exposure, and the chance to grow while contributing to GSK's mission of uniting science, technology and talent to get ahead of disease together. This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: Lead end-to-end change control for process, equipment, and facility changes, ensuring timely approvals and robust documentation. Investigate manufacturing deviations and quality events using structured root cause analysis and define effective corrective actions. Review batch and laboratory records for completeness and compliance with procedures and regulatory expectations. Support validation and qualification activities by linking change controls to DQ/IQ/OQ/PQ and related documentation. Maintain and improve Quality Management System processes, including CAPA, document control, and periodic product review inputs. Provide shop-floor coaching and practical guidance on good documentation practice, GMP, and data integrity.

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