Regulated Pharmaceutical Engineer

vor 22 Stunden


Visp, Schweiz Cpl Healthcare Vollzeit
About the Role

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.
Requirements:

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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