CQV Engineer – GMP Validation for Life Sciences

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

Benefits offered by this job

Certification reimbursement

Referral bonuses

Industry memberships reimbursed

Job summary

IPS - Integrated Project Services, LLC is seeking a CQV Engineer to join our team supporting Commissioning, Qualification and Validation for life sciences projects. The role focuses on cGMP-based services, including commissioning, qualification, validation, consulting, and related activities across pharmaceutical, biotech, and medical device sectors.

Responsibilities include writing cGMP-compliant C/Q/V documents, performing field activities such as FATs/SATs, witnessing tests, and compiling

Qualifications

• Bachelor of Science 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, FATS/SATs, SOPs).
• Perform field/site activities: attend/witness FATs and SATs, execute commissioning forms, and QA protocols.
• Read, understand, and apply IPS Best Practices and SOPs for compliant service delivery.
• Assist in deviation investigations and issue resolution during field execution.
• Provide timely feedback and reports to project leaders and managers.

Skills

CQV

Education

Bachelor of Science in Engineering

Job description

IPS - Integrated Project Services, LLC is seeking a CQV Engineer to join our team supporting Commissioning, Qualification and Validation for life sciences projects. The role focuses on cGMP-based services, including commissioning, qualification, validation, consulting, and related activities across pharmaceutical, biotech, and medical device sectors.

Responsibilities include writing cGMP-compliant C/Q/V documents, performing field activities such as FATs/SATs, witnessing tests, and compiling