CQV Engineer I — GMP Validation & Field Execution

IPS-Integrated Project Services; Lexington (KY); On-site; USD 60,000 - 80,000; Full time

Job summary

A global consulting and engineering firm is seeking a CQV Engineer in Lexington, Kentucky. The role involves performing cGMP compliance-based services, writing C/Q/V documents, and executing field/site activities. Candidates should have a Bachelor's degree in Engineering and ideally 0-2 years of experience in pharmaceuticals or related industries. This safety-sensitive position requires up to 100% travel to client sites, adhering to strict cleaning protocols in various environments, ensuring quality in compliance services.

Qualifications

• 0-2 years of relevant experience.
• Experience in Pharmaceutical, Biotech, Medical Device Design, Construction, or QA.

Responsibilities

• Write C/Q/V documents following established standards.
• Perform field/site activities for C/Q/V.
• Primary responsibilities include C/Q/V of equipment and systems.

Skills

cGMP compliance

Field activities

Report preparation

Understanding of regulatory requirements

Education

Bachelor of Science in Engineering

Job description

A global consulting and engineering firm is seeking a CQV Engineer in Lexington, Kentucky. The role involves performing cGMP compliance-based services, writing C/Q/V documents, and executing field/site activities. Candidates should have a Bachelor's degree in Engineering and ideally 0-2 years of experience in pharmaceuticals or related industries. This safety-sensitive position requires up to 100% travel to client sites, adhering to strict cleaning protocols in various environments, ensuring quality in compliance services.