Specialist QA - Validation, cGMP
AI Summary
A Specialist QA performs validation and quality assurance in a cGMP/biopharma setting, overseeing pharmaceutical process/system validation, project management, and driving conformance and continuous improvement.
About this role
Specialist QA - Validation, cGMP
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
Qualifications
• Bachelor degree in a science or engineering discipline
• No less than 5 years of experience in the pharmaceutical environment and validation
Additional Information
All your information will be kept confidential according to EEO guidelines.
Skills
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