HVAC & Clean Room CQV Engineer — 12‑Month Contract

Russell Tobin; Dublin; On-site; EUR 65,000 - 90,000; Full time

Job summary

Russell Tobin is recruiting for a CQV specialist to lead testing documentation for HVAC & Clean Rooms within a sterile drug production facility in Dublin. The role focuses on safety deliverables, CQV schedule management, and quality records to ensure compliance with GMP, EU, and FDA regulations.

Requirements include a Bachelor's degree in a scientific/engineering field and 3-5 years of CQV experience, with proficiency in Kneat or ValGenesis advantageous.

Qualifications

• Bachelor’s degree in a scientific, technical or engineering discipline.
• 3-5 years of C&Q experience including documentation preparation and execution.
• Experience implementing a CQV strategy and executing CQV testing from initiation to completion.
• Experience working in a diverse CQV team to deliver tasks safely, with quality and on time.

Responsibilities

• Development and execution of CQV testing documentation for HVAC & Clean Rooms for the Sterile Drug product facility.
• Meet key project deliverables for safety, CQV schedule management and quality of project documentation/electronic records for HVAC & Clean Rooms.
• Ensure GMP Clean Rooms, Cold Rooms and HVAC Equipment systems are tested in compliance with GMP, EU & FDA regulations and Global procedures.

Skills

CQV testing

Project management

Team collaboration

Documentation & execution

Education

Bachelor’s degree in scientific/engineering

Tools

Kneat

ValGenesis

Job description

Russell Tobin is recruiting for a CQV specialist to lead testing documentation for HVAC & Clean Rooms within a sterile drug production facility in Dublin. The role focuses on safety deliverables, CQV schedule management, and quality records to ensure compliance with GMP, EU, and FDA regulations.

Requirements include a Bachelor's degree in a scientific/engineering field and 3-5 years of CQV experience, with proficiency in Kneat or ValGenesis advantageous.