Job Description

Lonza Singapore is seeking a QA Specialist to support day‑to‑day quality assurance activities in a multi‑product cGxP contract manufacturing facility. The role involves ensuring compliance with SOPs and regulatory requirements, with responsibilities spanning batch record review, deviation handling, CAPA closure, and audits.

The ideal candidate holds a science degree, has GMP experience in biopharma, and can operate independently while collaborating with cross‑functional teams.

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