We have a current opportunity for a QA HVAC Documentation Specialist on a contract basis for one of our clients, a global science and technology company. The position will be based in the French-speaking part of Switzerland.
Missions:
- Collaborate with the HVAC project
- Participate to and approve the risk assessments
- Perform the quality review and approval of HVAC systems
- Review, approve and follow the CCPs
- Comply with all applicable regulations,
- Back-up of the QA CQV HVAC systems lead
Profile:
- At least 3 years work experience in Biotechnology/ Pharma
- Operational knowledge on CQV activities and standards
- Experience performing GMP and/or GEP documentation
- Ability to work collaboratively with cross functional team
- Ability to operate independently in his/her tasks
- Fluency in English
For further information about this position please apply by sending your CV and a confirmation of the right to work in Switzerland.
