CQV Engineer

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!