**
GSK is seeking a MSAT Product and Process Validation Specialist for its Marietta, PA facility, focusing on optimizing and validating manufacturing processes in vaccine production. The ideal candidate will have a background in biopharma, strong technical writing skills, and experience with regulatory requirements.
**
Job Summary
Develop, validate, optimize, and maintain robust manufacturing processes in our vaccine production facility to ensure process efficiency, consistency, and compliance with regulatory and quality standards.
Lead/Support design, tech transfer, and qualification of Incoming Materials (Chemicals and Single Use Systems), including Extractable and Leachable Assessments.
Partner with Site Operations, Quality, Engineering, Supply Chain, MSAT SMEs and Global teams to deliver compliant, practical solutions.
Matching Summary
Match Score: 75
**
GSK is seeking a MSAT Product and Process Validation Specialist for its Marietta, PA facility, focusing on optimizing and validating manufacturing processes in vaccine production. The ideal candidate will have a background in biopharma, strong technical writing skills, and experience with regulatory requirements.
**
Skills & Requirements
Must-have
Process validation lifecycle
Incoming material qualification
Root-cause analysis
Cross-functional collaboration
Technical writing and execution
Nice-to-have
Curious and open to learning
Willing to share knowledge
Ambitious for patients
Accountable for impact
Key Requirements
2+ years experience in vaccine/biopharma Incoming Materials
Bachelor Degree of Science or equivalent
Knowledge of regulatory requirements for Incoming Materials