CQV Engineer II — GMP Validation Specialist

IPS - Integrated Project Services, LLC; San Diego (CA); On-site; USD 79,750 - 106,300; Full time

Benefits offered by this job

Medical insurance

Dental insurance

401(k) plan with company match

Job summary

IPS - Integrated Project Services, LLC is seeking a CQV Engineer II to support the New Jersey region. This role involves compliance-based services such as commissioning, qualification, and validation within the life sciences sector. The ideal candidate will have a Bachelor's degree in Engineering and at least 2 years of relevant experience.

This position demands strong documentation skills and significant travel up to 100%. IPS offers a comprehensive benefits package, including medical, dental, and a 401(k) plan with company match.

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.
• Perform field/site activities related to commissioning and validation.
• Primary responsibilities include C/Q/V of equipment and systems.

Job description

IPS - Integrated Project Services, LLC is seeking a CQV Engineer II to support the New Jersey region. This role involves compliance-based services such as commissioning, qualification, and validation within the life sciences sector. The ideal candidate will have a Bachelor's degree in Engineering and at least 2 years of relevant experience.

This position demands strong documentation skills and significant travel up to 100%. IPS offers a comprehensive benefits package, including medical, dental, and a 401(k) plan with company match.