Regulated Pharmaceutical Engineer
vor 22 Stunden
Cpl Healthcare requires a Regulated Pharmaceutical Engineer to join our team in Visp, Switzerland. The successful candidate will be responsible for ensuring compliance and execution of CSV activities throughout the project lifecycle.
Responsibilities:- Develop and manage CSV documents according to company SOPs.
- Execute CSV tests and ensure adherence to project timelines in collaboration with Project Managers and CQV Leads.
The ideal candidate will have a technical degree (Bachelor's level) in Engineering or Applied Sciences, with postgraduate qualifications preferred. A minimum of 5+ years' experience in Commissioning, Qualification, and Validation (CQV), with a focus on CSV, is required.
Desirable Skills & Experience:
- Significant experience in automation and vertical integration, with expertise in data management under validated computer systems.
- Strong background in managing complex pharmaceutical projects, ideally within biologics (mammalian, CGT) or chemical manufacturing technologies.
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Performance Qualification
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CSV Engineer
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