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Senior Pharmaceutical Commissioning Validation Specialist
2 weeks ago
Senior Pharmaceutical Commissioning Qualification Validation Engineer
Job Summary:We are seeking a Senior CQV Engineer to perform commissioning, qualification, and validation of pharmaceutical facilities, utilities, and equipment. The ideal candidate will have experience in developing documentation for CQV activities and providing cGMP leadership and guidance.
Key Responsibilities:- Develop documentation for commissioning, qualification, and validation of pharmaceutical facilities, utilities, and equipment.
- Responsible for protocol writing and execution (field verification), and development of summary reports at client sites.
- Provide cGMP leadership and guidance for the integration and delivery of CQV services for Life Sciences clients.
- Bachelor's or Master's degree in a relevant science or engineering field, or equivalent years of hands-on experience.
- 5 – 12 years' experience performing commissioning and/or qualification activities in an FDA regulated industry.
- Excellent technical problem-solving and troubleshooting skills, with solid knowledge of typical project technical issues.
This role requires high attention to detail, ability to multi-task, and take initiative to accomplish assigned tasks accurately by established deadlines. The ideal candidate will be able to work independently, while quickly building and nurturing a project team.
