CQV Engineer II - Life Sciences Validation Pro

IPS-Integrated Project Services; New Jersey; On-site; USD 79,750 - 106,300; Full time

Benefits offered by this job

Comprehensive benefits package

401(k) plan with company match

Paid time off

Educational assistance

Job summary

IPS-Integrated Project Services is seeking a CQV Engineer II to join their team in New Jersey, focusing on cGMP compliance services in the life sciences industry. The ideal candidate will write and execute commissioning documents, perform field activities, and ensure compliance with IPS standards.

This role requires 2+ years of experience and offers a salary range between $79,750 and $106,300, depending on qualifications. Extensive travel is part of the job, with the potential for overnight stays at client sites.

Qualifications

• 2+ years of relevant experience in Pharmaceutical, Biotech, Medical Device Design, Construction.
• Experience in writing and execution of commissioning protocols.
• Knowledge of regulatory requirements for cGMP.

Responsibilities

• Write C/Q/V documents including commissioning forms and protocols.
• Perform field/site activities and witness FATs and SATs.
• Compile data and prepare reports for completed C/Q/V activities.

Skills

cGMP compliance

Commissioning

Validation

Problem solving

Education

Bachelor of Science in Engineering

Job description

IPS-Integrated Project Services is seeking a CQV Engineer II to join their team in New Jersey, focusing on cGMP compliance services in the life sciences industry. The ideal candidate will write and execute commissioning documents, perform field activities, and ensure compliance with IPS standards.

This role requires 2+ years of experience and offers a salary range between $79,750 and $106,300, depending on qualifications. Extensive travel is part of the job, with the potential for overnight stays at client sites.