You will support product and process compliance activities across a manufacturing site in the United States, working closely with operations, engineering, laboratory, regulatory, and quality colleagues
Job Summary
You will support product and process compliance activities across a manufacturing site in the United States, working closely with operations, engineering, laboratory, regulatory, and quality colleagues.
Responsibilities include leading end-to-end change control, investigating manufacturing deviations, reviewing batch records, and maintaining Quality Management System processes.
This role offers hands-on experience, cross-functional exposure, and the chance to grow while contributing to GSK’s mission of uniting science, technology and talent to get ahead of disease together.
Matching Summary
You will support product and process compliance activities across a manufacturing site in the United States, working closely with operations, engineering, laboratory, regulatory, and quality colleagues.
Skills & Requirements
Must-have
Product and process compliance
Quality systems management
Root cause analysis
GMP and GDP knowledge
Change control management
Nice-to-have
Practical problem solving
Clear communication
Commitment to patient safety
Cross-functional exposure
Shop-floor coaching
Key Requirements
Associate degree or equivalent experience
1+ year experience in regulated life science quality role
Experience with quality systems (change control, deviations, CAPA)