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GSK is seeking an MSAT Product and Process Validation Specialist for its Marietta, PA site to develop and maintain robust manufacturing processes for vaccines. The ideal candidate should have at least two years of experience in biopharmaceutical manufacturing, particularly with incoming materials, and possess strong technical and problem-solving skills.
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Job Summary
Develop, validate, optimize, and maintain robust manufacturing processes in a vaccine production facility to ensure efficiency, consistency, and compliance.
Lead investigations, deviations, root-cause analysis, CAPA, complaints, and gaps assessment for product, process, and incoming material performance issues.
Partner with Site Operations, Quality, Engineering, Supply Chain, MSAT SMEs, and Global teams to deliver compliant, practical solutions.
Matching Summary
Match Score: 75
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GSK is seeking an MSAT Product and Process Validation Specialist for its Marietta, PA site to develop and maintain robust manufacturing processes for vaccines. The ideal candidate should have at least two years of experience in biopharmaceutical manufacturing, particularly with incoming materials, and possess strong technical and problem-solving skills.
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Skills & Requirements
Must-have
Process validation lifecycle
Incoming material qualification
Technical writing and documentation
Risk-based approaches
Process optimization initiatives
Nice-to-have
Cross-functional collaboration
Technical problem-solving
Curious and open to learning
Ambitious for patients
Key Requirements
2+ years experience in vaccine/biopharma Incoming Materials
Bachelor Degree of Science or equivalent
Experience with technical writing
Knowledge of applicable regulatory requirements
Experience with process performance qualification strategies