Quality Systems & Data Manager
GSK
July 02, 2026
Remote friendly (Zebulon, NC)
United States
Operations
Position Summary
You will lead and strengthen quality systems that support safe, compliant and reliable manufacturing and laboratory operations.
Key Responsibilities
- Create and drive the Quality digital strategy with site and central functions, including smart manufacturing initiatives.
- Provide leadership and strategy for the site data integrity and governance program.
- Use lean six sigma methodologies to advance systemic quality improvements through the GSK production system.
- Ensure comprehensive training compliance, maintain up-to-date training records, and facilitate necessary training.
- Manage implementation of local updates to site quality digital systems (e.g., VQMS, MERP) using appropriate change management.
- Develop, implement, and monitor the Quality Improvement Plan; drive continuous improvement.
- Collaborate cross-functionally to align and integrate quality systems and processes.
- Develop and maintain quality documentation systems to ensure regulatory compliance, accessibility, and continuous improvement.
- Drive Quality Culture initiatives at the site.
Basic Qualifications (Required)
- Bachelor’s degree in a Scientific, Technical, Computer Science discipline or equivalent experience.
- 8+ years’ experience in commercial pharmaceutical manufacturing facility, including supervisory roles.
- Fundamental understanding of digital systems, continuous improvement tools, and lean six sigma.
- Expertise in digital quality, data integrity, and data governance.
Preferred Qualifications
- Knowledge of electronic quality management systems, data integrity frameworks, and regulatory expectations.
- Leadership experience, collaboration skills, and effective decision-making.
- Proficiency in data analytics and reporting.
Working model
Hybrid; expected to work on-site regularly with flexibility for remote work as agreed.
How to apply
Apply and tell how your experience will help improve processes and deliver high-quality results.
You will lead and strengthen quality systems that support safe, compliant and reliable manufacturing and laboratory operations.
Key Responsibilities
- Create and drive the Quality digital strategy with site and central functions, including smart manufacturing initiatives.
- Provide leadership and strategy for the site data integrity and governance program.
- Use lean six sigma methodologies to advance systemic quality improvements through the GSK production system.
- Ensure comprehensive training compliance, maintain up-to-date training records, and facilitate necessary training.
- Manage implementation of local updates to site quality digital systems (e.g., VQMS, MERP) using appropriate change management.
- Develop, implement, and monitor the Quality Improvement Plan; drive continuous improvement.
- Collaborate cross-functionally to align and integrate quality systems and processes.
- Develop and maintain quality documentation systems to ensure regulatory compliance, accessibility, and continuous improvement.
- Drive Quality Culture initiatives at the site.
Basic Qualifications (Required)
- Bachelor’s degree in a Scientific, Technical, Computer Science discipline or equivalent experience.
- 8+ years’ experience in commercial pharmaceutical manufacturing facility, including supervisory roles.
- Fundamental understanding of digital systems, continuous improvement tools, and lean six sigma.
- Expertise in digital quality, data integrity, and data governance.
Preferred Qualifications
- Knowledge of electronic quality management systems, data integrity frameworks, and regulatory expectations.
- Leadership experience, collaboration skills, and effective decision-making.
- Proficiency in data analytics and reporting.
Working model
Hybrid; expected to work on-site regularly with flexibility for remote work as agreed.
How to apply
Apply and tell how your experience will help improve processes and deliver high-quality results.