Jobs and Careers
GS

Regulatory Compliance Lead

GSK
Zebulon, United States, United Statesfull_timeVerifiedPosted 22 Jun 2026

About the role

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 product. 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:

This role leads a team of professionals acting as advisor, facilitator and team member regarding regulatory compliance and pertinent quality systems for all aspects of the manufacturing, testing, storage and distribution of pharmaceutical products. This position will provide guidance and training to new and existing employees and assist them with decision making. You will lead regulatory compliance activities across US operations. You will work with quality, manufacturing, and technical teams to ensure compliance with regulations and company standards. Your team values clear thinking, practical problem solving, and collaboration. You will have the chance to grow your skills, shape compliance practices, and make a measurable impact on patient safety and public health. Join us to unite science, technology and talent to get ahead of disease together.

Responsibilities:

This role will provide you the opportunity to lead key activities to progress your career. You will lead regulatory compliance programs and ensure alignment with US and global regulatory requirements. Support inspection readiness including responses to regulatory authority requests and audits. Manage regulatory risk assessments and drive corrective and preventive actions to closure. Collaborate with cross-functional teams to implement compliance plans and improve processes. Prepare clear reports and metrics for leadership on compliance status and improvement initiatives. Coach and influence colleagues to build a proactive compliance culture across the organization.

  • Ensuring all proposed technical changes are properly assessed via the Change Control System, providing guidance to the impact on regulatory submissions, RIS (Regulatory Implementation Strategy) and using this information to assist change owners in the assessment of scope for the change.   

  • Ensures site representation in meetings requiring regulatory input and updates. (i.e. PTRT, CoPs, Change Control Panel,  

  • Manage the implementation of registered commitments to ensure continuous compliance and success in global regulatory authority inspections (e.g. FDA ). 

  • Coordinates efforts with GSK Regulatory Affairs, LOCs and other business departments to assure all mandatory licenses and registrations are kept current and in compliance with relevant health authority requirements.   

  • Oversee the management of Quality Agreements (QA and iQA) and Quali

Apply for this role

Generate a tailored application kit with a matched cover letter, interview prep, and CV highlights — in under 60 seconds.

Apply Now →Generate Application Kit

Free account required — sign up in 30s

Company

GSK

View company profile →