HVAC Engineer

Development and execution of CQV testing documentation for HVAC & Clean Rooms for the Sterile Drug product facility.Responsible for meeting key project deliverables for safety, CQV schedule management and quality of project related documentation/electronic records for HVAC & Clean Rooms assigned.Responsible for ensuring GMP Clean Rooms, Cold Rooms and HVAC Equipment systems are tested in compliance with good manufacturing practices, company policies and EU & FDA regulations and client procedures.Risk Management - Identifies and categorizes CQV risks according to impact on commissioning and qualification. Generation of action plans to mitigate qualification risks.

What you’ll need:

Bachelor’s degree in a scientific, technical or engineering disciplineExtensive C&Q experience to include both documentation preparation and executionDemonstratable capacity to implement a project CQV strategy, effectively execute the CQV testing approach for assigned from initiation to completion.Demonstrable experience of performing as part of diverse team of CQV professionals/ contractors to deliver on tasks safely, with quality focus, on time and within budget.

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