CQV Engineer: GMP Validation & Commissioning

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

Benefits offered by this job

Medical, dental and vision insurance

401(k) with company match

Paid time off and holidays

Flexible spending accounts

Educational assistance

Certification pay and referral bonuses

Travel opportunities

Job summary

IPS is seeking a CQV Engineer to support Commissioning, Qualification and Validation of technically complex facilities in life sciences. You will perform cGMP-compliance based C/Q/V services and may perform standalone commissioning for non-FDA regulated clients.

Responsibilities include writing C/Q/V documents, witnessing FATs/SATs, and compiling data for reports. The role requires a Bachelor of Science in Engineering and 2+ years of related experience.

Qualifications

• Bachelor's degree in Engineering required.
• 2+ years of relevant experience in CQV, GMP, pharma.
• Experience with GMP utilities, equipment, systems, and software preferred.

Responsibilities

• Write C/Q/V documents following established standards and templates (e.g., Protocols, Reports, SOPs).
• Perform field/site activities: attend and witness FATs/SATs, execute C/Q/V protocols, and verify drawings.
• Lead C/Q/V of equipment and systems including CSV and automation for pharma/biotech/medical device projects.

Skills

CQV experience

Documentation

Field execution

Education

Bachelor of Science in Engineering

Job description

IPS is seeking a CQV Engineer to support Commissioning, Qualification and Validation of technically complex facilities in life sciences. You will perform cGMP-compliance based C/Q/V services and may perform standalone commissioning for non-FDA regulated clients.

Responsibilities include writing C/Q/V documents, witnessing FATs/SATs, and compiling data for reports. The role requires a Bachelor of Science in Engineering and 2+ years of related experience.