Location: Visp, Switzerland
Company: Lonza
Employment Type: Full-Time

Shape the future of the pharmaceutical and biotech industries with Lonza. We are seeking a CQV Engineer to join our Global Engineering team in Visp. In this role, you will be instrumental in executing commissioning, qualification, and validation (CQV) activities to ensure seamless project delivery in a regulated environment.

Responsibilities:

• Execute and approve Design Qualification (DQ), Installation Qualification (IQ), Operational Qualification (OQ), and commissioning activities for critical systems.
• Develop and manage system boundaries and GMP risk assessments.
• Oversee vendor testing and ensure adherence to project guidelines.
• Perform system checks, PSSR write-ups, and ensure compliance with cGMP standards.
• Collaborate with cross-functional teams to ensure timely project execution.
• Document all activities in alignment with regulatory and project requirements.

Minimum Requirements:

• Bachelor's degree in Life Sciences or Engineering.
• 2+ years of experience in CQV activities within the pharmaceutical/biotech industry.
• Strong knowledge of clean utilities and systems validation (DQ, IQ, OQ, commissioning).
• Familiarity with DeltaV (Emerson) and control systems.
• Excellent written and verbal communication skills in English.
• Proficiency in cGMP standards and regulatory requirements.
• Ability to work independently and meet project deadlines.

Preferred Requirements:

• Proficiency in German is highly desirable.
• Familiarity with Lonza's CQV approach and experience with COMOS/KNEAT platforms.
• Strong knowledge of biopharmaceutical processes.
  
  

Ready to take the next step? Join Lonza and make a difference in life sciences.