Job Summary
The DS2 CQV Engineer will be responsible for the execution of commissioning and qualification of process equipment and utilities within the DS2 project scope. This role will involve working closely with Quality, Engineering, and CQV teams to ensure that systems, equipment, and processes are designed, installed, commissioned, and qualified to agreed specifications.
Key Responsibilities
* Perform shakedown and commissioning/qualification of systems
* Participate in construction system completion walkdowns
* Generate CQV documents at project level and for specific equipment/systems Liaising with Quality, Engineering & CQV to align on Critical parameters & document content Track & confirm closure of actions items identified from walkdowns FAT HAZOP Design Qualification
* Maintain a strong interface with Automation & Engineering teams to ensure information flow meets needs resolving issues as they arise
About Us:
The ideal candidate will have a B.Sc./B.Eng degree in an engineering discipline (with particular emphasis mechanical or process engineering) Minimum 4 years experience from biotechnology or pharmaceutical GMP manufacturing/CQV environment Demonstrated ability to work on own initiative proactively responding business needs Excellent interpersonal communication skills Familiarity with Delta-V Navis Works an advantage."],