CQV Engineer - GMP Validation for Life Sciences

IPS - Integrated Project Services, LLC; Emeryville (CA); On-site; USD 67,050 - 111,750; Full time

Benefits offered by this job

Pay for certifications

Referral bonuses

Industry memberships paid

Job summary

IPS – Integrated Project Services, LLC is seeking a CQV Engineer to support commissioning, qualification and validation activities for technically complex facilities in life sciences. You will perform cGMP-based services and follow IPS standards and regulatory requirements, including standalone commissioning for non-FDA-regulated clients.

The role involves writing C/Q/V documents, executing field activities, witnessing FATs/SATs, and preparing reports.

Qualifications

• 2+ years of relevant experience in CQV/validation
• Experience in Pharmaceutical, Biotech, Medical Device design or validation is preferred
• Ability to write and execute GMP documentation and protocols

Responsibilities

• Write C/Q/V documents using established IPS templates
• Perform field activities including FATs, SATs, and system walkdowns
• Compile data and prepare C/Q/V reports and ETOPs
• Assist in deviation investigations and issue resolution during field work
• Support commissioning, qualification, and validation of equipment and systems

Skills

CQV knowledge

Attention to detail

Education

Bachelor of Science in Engineering

Tools

FATs/SATs protocols

Job description

IPS – Integrated Project Services, LLC is seeking a CQV Engineer to support commissioning, qualification and validation activities for technically complex facilities in life sciences. You will perform cGMP-based services and follow IPS standards and regulatory requirements, including standalone commissioning for non-FDA-regulated clients.

The role involves writing C/Q/V documents, executing field activities, witnessing FATs/SATs, and preparing reports.