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Melbourne, Melbourne Region💼 Full-time🗓 2026-06-18 → 2026-08-07

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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