Onsite training is provided in the QA Auditor's job duties, which include: Perform in-house line audits of pharmaceutical filling and packaging operations; review manufacturing activities and documentation for compliance with SOPs; perform line clearances, in-process, and end-item inspections; review and apply specifications for acceptance of in-coming packaging components, raw materials, and finished products; generate, review, and issue batch production records; release materials & components for use in production; organize and issue printed materials to production; monitor & interpret charts and gauges; log book review, issuance, and archival. Successful candidates will be highly motivated, self-starters with knowledge of contemporary cGMP practices and procedures. Good written and oral communication is essential. Technical writing is a plus.
EDUCATION & EXPERIENCE: Associates degree in Science, or equivalent is required. Bachelors degree in Science, or equivalent is preferred. 1-4 years' experience in or Quality Assurance or Manufacturing, preferably in an FDA regulated environment. Working knowledge of cGMPs is preferred.
Knowledge, Skills & Abilities of QA Auditor I/II/Senior include:
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