CQV Engineer – GMP Commissioning & Validation

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

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

401(k) with match

Paid time off

Holidays

Educational assistance

Certification support

Referral bonuses

Overtime pay after 40h

Job summary

IPS is seeking a CQV Engineer to support commissioning, qualification and validation for life sciences projects. You will perform cGMP-compliance services, develop and execute C/Q/V protocols, and prepare data packages for completed activities.

The role requires a BS in engineering and 2+ years of relevant experience, with up to 100% travel. IPS offers benefits and opportunities in a global life sciences environment.

Qualifications

• BS in engineering required.
• 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 (protocols, reports, SOPs).
• Perform field activities: witness FATs/SATs, execute C/Q/V protocols, walkdowns, data package preparation.
• Assist in deviation investigations and issue resolution during field execution.

Skills

CQV

cGMP

Education

Bachelor of Science in Engineering

Job description

IPS is seeking a CQV Engineer to support commissioning, qualification and validation for life sciences projects. You will perform cGMP-compliance services, develop and execute C/Q/V protocols, and prepare data packages for completed activities.

The role requires a BS in engineering and 2+ years of relevant experience, with up to 100% travel. IPS offers benefits and opportunities in a global life sciences environment.