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Commissioning qualification & validation (CQV) Engineer
| Hours | Full-time, Part-time |
|---|---|
| Location | Swiftwater, Pennsylvania |
About this job
Job Description
This is a contract assignment with a global pharmaceutical company.
BSc/BEng plus previous experience in CQV field or equivalent combination of education and experience. Experience in pharmaceutical/biopharmaceutical industry or related industry/manufacturing environment. Areas of experience: plant utilities, clean utilities, CIP, SIP, Fill Finish, HVAC, Filling lines, CTUs, component prep equipment, formulation. Well-developed communication skills, both verbal and written.
Essential Duties and Responsibilities:
• Writes and executes commissioning, qualification, & validation protocols for facilities utilities, equipment, and computerized systems
• Writes final reports
• Resolves protocol discrepancies and deviations
• Reviews vendor generated validation protocol packages
• Responsible for the generation of complex protocols using a risk based approach that meets current regulatory requirements and industry practices
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