QA Associate
Core
QA Associate supporting manufacturing operations in pharmaceutical/medical device sector through document review, change controls, CAPA, and validation.
Role type
QA Associate
Builds
GMP-compliant manufacturing processes and documentation
Domain
Pharmaceutical/Medical Device Manufacturing
Deliverable
client delivery
Required skills
QA within Pharmaceutical/Medical Device, CAPA & deviations, document review, GMP knowledge, validation protocols
Preferred skills
Science or Engineering tertiary qualification, problem solving, cross-functional collaboration
Technologies
GMP, CAPA, validation protocols
Responsibilities
Perform routine quality walkthroughs of GMP facility operations, review & approve GMP documentation, review validation protocols, engage with manufacturing for quality problem solving
Seniority
Individual Contributor
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