Product Release Leader

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 To provide operational quality support and oversight to all GMP areas including Oral Solid Dose (OSD), Metered Dose Inhaler (MDI) and Multi‑Dose Powder Inhaler (MDPI), Laboratories, Warehouse, and Facility/Utility areas. Responsibilities This role will provide you the opportunity to lead key activities to progress your career. These responsibilities include some of the following: Provide quality oversight for GMP areas including Oral Solid Dose, Metered Dose Inhaler (MDI) and Multi‑Dose Powder Inhaler (MDPI), Laboratories, Warehouse, and Facility/Utility areas. Maintain presence across area of responsibility and be the first line of contact to support initial management of quality issues. Accountable for quality decision making via work order assessments, atypical comments, and initial impact assessment for deviations. Responsible for review, release and second check of batch record documentation for compliance to cGMPs, SOPs, and internal and regulatory requirements. Also ensuring that all GMP documentation and records follow Good Documentation Practice (GDP) by adhering to ALCOA++ principles for data integrity through both review and end‑user support. Provide timely guidance during GMP activities to proactively detect potential quality issues through active observation in real‑time, allowing for timely interventions to prevent deviations and defects. Support and/or lead problem solving / root cause analysis and CAPA identification. Perform a spot‑check of activities across defined GMP areas to ensure compliance with quality standards that includes production, testing, cleaning and maintenance activities. Check that facilities are being maintained in a good state in line with local housekeeping standards and any deviation from the standards are escalated and support timely implementation of remedial actions. Collaborate with cross‑functional teams to resolve quality issues, implement corrective/preventive actions (CAPAs) and support and/or lead continuous improvement efforts. Check that facilities are being maintained in a good state in line with local housekeeping standards and any deviation from the standards are escalated and support timely implementation of remedial actions. Role model the GPS standards and foster a Quality Starts with Me (QSWM) culture by providing coaching to employees on the importance of following procedures, doing the right thing and explaining the why and the impact non‑compliance can have on product quality and patient safety. Communicate effectively with team members, escalate issues to production and quality team/lead and provide on‑call support as required. Create, review and second check certificates (CoA, CoC) in alignment with market requirements and GSK standards. Basic Qualifications Bachelor’s Degree and 4+ years of GMP pharmaceutical experience. 4+ years of Pharmaceutical Manufacturing, Quality, QC experience or similar and able to apply Quality Management Systems (QMS) and GMP principles to day‑to‑day role. Experience working with quality systems such as deviations, CAPA, change control, and document control. Preferred Qualifications Bachelor’s degree in a scientific, engineering, or quality discipline. Must be able to work independently, but also be a strong team player. Good knowledge of cGMP's and other Regulatory requirements. Demonstrate initiative, think critically, analytical problem‑solving skills and build strong collaborative relationships across the organization. Excellent organizational skills and attention to detail while being able to adapt to change; ability to prioritize work effectively to deliver to expectations. Must be flexible, adaptable and a strong team player that fosters and promotes GSK Values, Behaviors and Strategies. A sound knowledge of pharmaceutical compliance requirements and the ability to interpret and translate to the Site environment. Proficient with IT applications, i.e. MERP, Microsoft Office, Power BI, VQD. Ability to think strategically. Demonstrated collaboration, negotiation and conflict resolution skills. Well‑developed interpersonal skills and decision‑making capabilities with the ability to resolve conflict and influence different levels of the Site and Quality organization. Ability to deliver clear communications (both verbally and written), coach others, foster a Quality Starts with Me (QSWM) culture and work with a spirit of continuous improvement. About the Zebulon Site The Zebulon site is a global supplier of Respiratory and Solid Dose medicines and the largest GSK Pharmaceutical secondary manufacturing site in North America. The site is located less than 30 minutes from Raleigh, Wendell, Knightdale, Rocky Mount, Wilson, and Wake Forest. Equal Opportunity Employer 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. #J-18808-Ljbffr GlaxoSmithKline