GSK
Quality Technical and Validation Manager
USA - Pennsylvania - Marietta · On-site · Manager · Full-time · Posted Jul 31, 2026
- Experience
- 10+ years in pharmaceutical or biotechnology industry; 5+ years of leadership experience.
- Education
- Bachelor’s degree in a relevant scientific or engineering discipline.
About the job
Leads site quality oversight of GxP validation, qualification, and lifecycle management for manufacturing, laboratory, equipment, and computer systems, including new product transfers and regulatory inspections.
What you'll do
- Oversee validation and qualification activities for processes, equipment, facilities, and systems, ensuring GxP and regulatory compliance.
- Review and approve technology-transfer activities and validation protocols; manage related change-control requirements.
- Monitor validation data, support audits and inspections, and oversee laboratory applications, methods, automation, and CSV compliance.
What they ask for
- Bachelor’s degree in a relevant scientific or engineering discipline.
- 10+ years of experience in the pharmaceutical or biotechnology industry, with responsibility/accountability for decisions and outcomes.
- 5+ years of leadership experience.
- Experience developing, approving, and executing process and equipment lifecycle management programs and their protocols and reports.
Nice to have
- Advanced degree in a relevant scientific or engineering discipline.
- Quality assurance or validation certification (e.g., ASQ, ISPE).
Tools
GMP, FDA, EMA, ICH, Six Sigma, Lean, CSV
AI focus
The posting describes AI as part of GSK’s broader smart-manufacturing direction, but does not specify AI work for this role.
Model-written summary · the original posting is authoritative