Product Release Leader

Biopharma Careers; Zebulon (GA); On-site; USD 90,000 - 130,000; Full time

Job summary

GSK US in Zebulon seeks an experienced QA professional to provide operational quality oversight across GMP areas, ensuring adherence to cGMP standards and GDP data integrity. You will review documentation, release products, and lead CAPA and continuous improvement initiatives.

The role requires a Bachelor’s degree in a scientific/engineering/quality discipline and 4+ years in pharmaceutical manufacturing, quality, or related fields. On-site work with potential night/weekend coverage.

Qualifications

• Bachelor’s Degree and 4+ years of GMP pharmaceutical experience.
• Experience with deviations, CAPA, change control, and document control.
• Able to apply QMS and GMP principles to day-to-day role.

Responsibilities

• Provide quality oversight for GMP areas including OSD, MDI and MDPI, Laboratories, Warehouse, and Facility/Utility areas.
• First line of contact for initial management of quality issues and deviations.
• Review, release and second check of batch records for cGMPs and GDP data integrity.
• Provide guidance during GMP activities to detect potential quality issues and support CAPA identification.
• Spot-check activities to ensure compliance and escalate deviations for timely remediation.
• Collaborate with cross-functional teams to implement corrective/preventive actions and continuous improvement.

Skills

Data Integrity

Detail‑Oriented

Digital Fluency

GxP Regulations

Influencing

Lean Management

Pharmaceutical Regulatory Compliance

Problem Solving

Quality Assurance

Risk Awareness

Technical Writing

Education

Bachelor’s degree in scientific/engineering/quality

Tools

MERP

Microsoft Office

Power BI

VQD

Job description

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

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.

Ensure adherence to cGxP standards and procedures through the independent oversight of GxP processes.

Review and release products that are manufactured and/or packaged in compliance with local and regulatory requirements.

Improve the effectiveness of quality in preventing /identifying and addressing quality issues by enabling a strong quality culture and leading continuous improvement efforts.

Maintain presence and be accountable for quality decision-making and quality escalations to all GMP operational areas.

Responsibilities

• 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, elevate 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.

Why You?

Work arrangement: This role will require 100% on-site for hands‑on release activities and inspections. Some Nights and Weekends will be expected with this role.

Basic Qualification

• 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 Qualification

• 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

GSK’s Zebulon site is a global supplier of Respiratory and Solid Dose medicines to patients around the globe and the largest GSK Pharmaceutical secondary manufacturing site in North America. The site is located less than 30 minutes from downtown Raleigh, Wendell, Knightdale, Rocky Mount, Wilson, and Wake Forest.

Key differentiators about GSK and Zebulon

• Our commitment to inclusion is seen as a critical advantage of ours
• Our focus on cultivating a positive work environment that cares for our employees
• Demonstrated opportunities for continued career growth driven by individual ambition
• Leaders that care about their teams and growth of both individuals and the company
• A priority focus on Safety and Quality
• Clean and GMP compliant work environment
• Onsite cafeteria
• Onsite gym
• Temperature‑controlled climate
• Licensed, onsite Health & Wellness clinic

What we value

We look for people who act with integrity, put patients first, and work well with others.

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 [e-mail]

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.