CQV Engineer II: GMP Validation for Life Sciences

IPS-Integrated Project Services; Emeryville (CA); On-site; USD 96,000 - 129,000; Full time

Job summary

IPS-Integrated Project Services in Emeryville, CA is seeking a CQV Engineer II to perform commissioning, qualification, and validation activities for life sciences facilities.

You will write and witness CQV documents, conduct field activities, and support CSV/automation projects, with up to 100% travel as required. A BS in Engineering and 2+ years of relevant experience in pharma/biotech/medical devices are expected.

Qualifications

• Bachelor's degree in Engineering.
• 2+ years of relevant experience.
• Experience in Pharmaceutical, Biotech, Medical Device Design, Construction, Commissioning, Validation, or QA.

Responsibilities

• Write C/Q/V documents following established standards and templates (e.g., Protocols, SOPs).
• Perform field/site activities including witnessing FATs/SATs and commissioning tests.
• Compile data and prepare reports for completed C/Q/V activities and support deviation investigations.

Education

Bachelor of Science in Engineering

Job description

IPS-Integrated Project Services in Emeryville, CA is seeking a CQV Engineer II to perform commissioning, qualification, and validation activities for life sciences facilities.

You will write and witness CQV documents, conduct field activities, and support CSV/automation projects, with up to 100% travel as required. A BS in Engineering and 2+ years of relevant experience in pharma/biotech/medical devices are expected.