CQV Professional – Lab and Facilities (CDMO) Are you a seasoned professional with extensive technical expertise in CQV? We are looking for CQV Engineers to join our client's team in Visp and Stein on a contract basis. The roles require a deep understanding of Qualification, Commissioning, and verification of both lab equipment and facilities.
Key Responsibilities:
Lead and execute commissioning, qualification, and validation (CQV) activities for laboratory equipment, cleanrooms, and critical facility systems (e.g., HVAC, utilities, and water systems).
Develop, review, and approve validation protocols, reports, and documentation to ensure compliance with regulatory standards and industry best practices.
Troubleshoot and resolve CQV-related issues, collaborating with engineering, quality, and operations teams to drive project success.
Must Haves:
Bachelor’s degree in Engineering, Life Sciences, or related field with 3+ years of experience in CQV for laboratory and facility systems.
Strong knowledge of regulatory requirements (e.g., cGMP, ICH Q9, Q10) and validation lifecycle for pharmaceutical/biotech facilities.
Proven ability to manage multiple projects simultaneously with excellent communication and problem-solving skills.
If you’re passionate about delivering high-quality solutions and thrive in a fast-paced CDMO environment, we invite you to apply and make an impact!
Seniority level Mid-Senior level
Employment type Contract
Job function Science and Engineering
Industries: Pharmaceutical Manufacturing
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