You will ensure manufacturing facilities, processes, systems and methods meet regulatory and good manufacturing practice expectations
Job Summary
You will ensure manufacturing facilities, processes, systems and methods meet regulatory and good manufacturing practice expectations.
This role offers growth, meaningful impact and the chance to help advance GSK’s mission of uniting science, technology and talent to get ahead of disease together.
We are committed to creating an inclusive workplace and providing equal opportunities for all applicants.
Matching Summary
You will ensure manufacturing facilities, processes, systems and methods meet regulatory and good manufacturing practice expectations.
Skills & Requirements
Must-have
cGMP and regulatory requirements
validation plans, protocols, reports
assess validation impact
quality oversight to validation projects
subject matter expert during audits
Nice-to-have
agile working culture
advance GSK’s mission
meaningful impact
solve problems
manage risk
Key Requirements
Bachelor’s degree or equivalent experience
Minimum 2 years’ experience
Practical knowledge of cGMP
Experience authoring and approving validation documents