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You will be in charge of the qualification of equipment related to production for a major company in the life sciences Industry.
Your main tasks will be (not exhaustive list) to:
* Conduct CQV activities focusing on qualification of manufacturing/production equipment (CIP equipment is a plus),
* Coordinate the installation and validation,
* Write and execute and/or supervise the execution of tests (IQ, OQ, PQ),
* Manage non-conformities and change.
PROFILE:
* You have a degree in Life Sciences, engineering or equivalent by experience.
* You have at least 3 years of experience in the qualification of production, manufacturing or packaging equipment in the Life Sciences Industry (biotech is a plus).
* You are used to working in a regulatory environment and have strong knowledge of regulatory standards related to pharmaceutical or biotechnology environment (GMP, GLP, ICH, 21 CFR, etc.).
* You speak fluent English.
* You have strong communication skills and analytical thinking.
* Your social skills enable you to work in a team; you are an autonomous person in your activities.
Only applicants with Swiss or EU/EFTA citizenship or applicants with an existing and valid residence and work permit in Switzerland will be considered.
Seniority level
Associate
Employment type
Full-time
Job function
Consulting, Engineering, and Manufacturing
Industries
Biotechnology Research and Pharmaceutical Manufacturing
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