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GMP Equipment Validation Specialist
Job in
Newbury Park, Ventura County, California, 91320, USA
Listed on 2026-07-18
Listing for:
Akraya
Full Time
position Listed on 2026-07-18
Job specializations:
-
Pharmaceutical
Pharmaceutical Manufacturing, Pharma Engineer -
Quality Assurance - QA/QC
Job Description & How to Apply Below
Location: Newbury Park
GMP Equipment Validation Specialist
This role is responsible for ensuring GMP equipment remains validated and compliant through periodic reviews. You will collaborate with various departments to assess equipment performance, maintenance, and lifecycle. The position requires detailed documentation and analysis to maintain regulatory standards in a pharmaceutical setting.
Key Responsibilities:
- Conduct periodic reviews of GMP equipment.
- Evaluate equipment documentation and performance history.
- Prepare and revise review reports.
- Liaise with cross-functional teams to address equipment issues.
- Track and report on review progress and metrics.
Must-Have Skills:
- Commissioning/Qualification/Validation experience
- GMP environment experience
- Biotech/pharmaceutical manufacturing equipment knowledge
Experience in the pharmaceutical or biotech industry is required, with a focus on roles related to commissioning, qualification, and validation of manufacturing equipment.
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