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Aequor Technologies

Specialist QA - Validation, cGMP

Aequor Technologies · Woburn, MA, United States

ContractOn-sitePosted 6 November 2026
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Job description

Engineering Job Title- Specialist QA Location- Woburn, MA Duration - 12 months with possible extension Key Skills - QA Pharma, Bio, biopharma, cGMP, validation, conformance, CAPAs, Change Bio-pharma space / Biologics . M-F onsite •    Knowledge in cGMP / GMP manufacturing and technical knowledge in validation of pharmaceutical processes/systems/equipment •    Project Management and organizational skills, including ability to follow assignments through to completion Direct: 732-339-3518 - Ext 2065 •    Bachelor degree in a science or engineering discipline •    No less than 5 years of experience in the pharmaceutical environment and validation All your information will be kept confidential according to EEO guidelines.

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