Job description

• Develop and execute validation protocols to ensure processes, instruments and/or facilities are compliant with regulatory standards.
  
  
• Utilities: commissioning and qualification of utilities (ex. purified water systems, clean steam systems, HVAC systems, and compressed air systems).
  
  
• Equipment: commissioning and qualification of biotechnology equipment (Ex: reactors, fermentation systems, downstream processing equipment, and cell culture systems).
  
  
• Cleaning: validation and qualification of cleaning process/equipments (Ex. procedure development, protocol preparation, sampling plan design, validation execution, verification and monitoring).
  
  
• Contribute to documentation of the CQV activities.
  
  
• Collaborate with cross-functional teams to optimize processes.
  
  
• Implement continuous improvement initiatives.

Your profile

• Applied knowledge of international pharmaceutical regulations and standards

• Demonstrated effective verbal and written communication skills in French and English (minimum B1/B2)

• Experience in one or more of the mentioned CQV specialties.

• Ability to work independently and collaboratively in a fast-paced, team-oriented environment.

• Willingness to travel within Switzerland. 

Benefits:

• Between 30% and 70% remote work in agreement with your manager and client needs (40% for cross boarders due to tax regulation)

• Options to order ergonomically proven equipment (monitor & chair) for your home-office premises

• Support for trainings, formation upon agreement with the manager

• Contribution on gym subscription

• Trust-based managerial culture

• Team rituals and get togethers

We look forward to receiving your application. Capgemini Engineering only accepts direct applications (no recruitment agencies).

Due to Swiss regulations we only consider Swiss or EU/EFTA applicants or applicants with a valid work permit.