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CQV Engineer

CQV Engineer

LocationVevey, Switzerland
Business SectorBiotechnology
Contact email
Job ref24732
Published3 days ago

In partnership with our global biopharmaceutical client in Vevey, Switzerland, we are looking for an experienced CQV engineer. The project is expected to last 6 months.

 

ROLE

 
  • Responsible for executing Commissioning, Qualification, and Validation (CQV) protocols to ensure compliance with established standards and procedures.

  • Carry out commissioning activities according to predefined check-lists, ensuring all systems and equipment meet operational requirements.

  • Monitor and coordinate with suppliers.

  • Utilize systems such as Valgenesis, Trackwise, and Mango to manage and track qualification processes effectively.

  • Ensure that all qualifications are completed within specified deadlines to avoid compliance issues.

  • Provide regular updates on ongoing qualifications and those scheduled for completion, ensuring clear communication with stakeholders.

 

PROFILE

 
  • 2+ years of experience in CQV within biopharmaceutical manufacturing

  • Experience with laboratory equipment

  • Dynamic & fast learner, autonomous and flexible

  • Knowledge on systems: Valgenesis, Trackwise, and Mango. 

 

PRACTICALITIES

 
  • Project duration: 1st July - 31st September 2025 (extendable until the end of the year)

  • 100% on-site

  • English a must, French highly preferred


Interested? Know someone that could be? Don’t hesitate to let me know on v.niesov@panda-int.com to find out more!