CQV Engineer: GMP Validation & Field Execution (Travel)

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

Benefits offered by this job

Medical insurance

Dental and vision insurance

401(k) plan with company match

Paid time off and holidays

Educational assistance

Job summary

IPS – CQV Engineer is a role within IPS that supports Commissioning, Qualification and Validation activities for life sciences facilities. The engineer will perform cGMP-based CQV services, write CQV documents, conduct field activities, and ensure compliance with IPS standards and regulatory requirements.

This position involves extensive travel to client sites as needed. Required is a Bachelor of Science in Engineering with 2+ years of relevant CQV experience and exposure to GMP utilities,

Qualifications

• Bachelor of Science in Engineering is required.
• 2+ years of relevant experience in CQV/validation.
• Experience in Pharmaceutical, Biotech, Medical Device Design, Construction, Commissioning, Validation, or QA is preferred.

Responsibilities

• Write C/Q/V documents following established IPS templates (PQC reports, SOPs, URS/FRS/DDS).
• Perform field/site activities: attend/witness FATs/SATs, execute C/Q/V protocols, walkdowns, and data packages.
• Assist in deviation investigation and issue resolution during field execution.
• Provide feedback and reports to project leaders and management on status and issues.

Skills

CQV experience

Education

Bachelor of Science in Engineering

Job description

IPS – CQV Engineer is a role within IPS that supports Commissioning, Qualification and Validation activities for life sciences facilities. The engineer will perform cGMP-based CQV services, write CQV documents, conduct field activities, and ensure compliance with IPS standards and regulatory requirements.

This position involves extensive travel to client sites as needed. Required is a Bachelor of Science in Engineering with 2+ years of relevant CQV experience and exposure to GMP utilities,