CQV Engineer II: GMP Validation & Commissioning

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

Job summary

IPS is seeking a CQV Engineer II to join our Emeryville, CA team. The role focuses on cGMP-based commissioning, qualification, validation, and related consulting services for life sciences facilities. You will perform field activities, witness FATs/SATs, and prepare data packages for completed C/Q/V activities.

Qualifications include a BS in Engineering and 2+ years of relevant experience in pharmaceuticals or biotech. Travel up to 100% is required as needed by projects.

Qualifications

• Bachelor of Science in Engineering.
• 2+ years of relevant experience in CQV/validation/commissioning.
• 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, Specifications).
• Perform field/site activities including witnessing FATs/SATs and execution of C/Q/V protocols.
• Read, understand, and apply IPS Best Practices and SOPs for compliance services.

Education

Bachelor of Science in Engineering

Job description

IPS is seeking a CQV Engineer II to join our Emeryville, CA team. The role focuses on cGMP-based commissioning, qualification, validation, and related consulting services for life sciences facilities. You will perform field activities, witness FATs/SATs, and prepare data packages for completed C/Q/V activities.

Qualifications include a BS in Engineering and 2+ years of relevant experience in pharmaceuticals or biotech. Travel up to 100% is required as needed by projects.