Specialist QA - Validation, cGMP
Aequor
Apply to this jobEngineering
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.
Summary
Validate pharmaceutical processes, ensure cGMP compliance, manage CAPAs and change controls
Job title
Specialist QA - Validation, cGMP
Experience level
5+ years
Industry
pharmaceutical
Location requirements
Woburn, MA, on-site, no remote work allowed
Salary
Not specified
Management role
No
Required skills
Preferred skills
Specializations
Structured locations inferred from the posting.
Woburn, MA, USA