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C&Q Engineers
Employer undisclosedRole managed by a recruiter
Engineer managing design reviews, testing, and qualification for pharma production facility.
Attend FAT and execution of agreed testing protocols and sign off on permission to ship forms.
Track and confirm closure of actions items identified through FAT, HAZOP, Design Qualification and other reviews.
Generate CQV documents at project level and for specific equipment/systems. Liaising with Quality, Engineering and CQV to align on Critical parameters and document content.
Participate in design document reviews and ensure that quality aspects are included in design.
Participate in construction system completion walkdowns.
Perform shakedown and commissioning and qualification of systems.
Maintain a strong interface with the Automation and Engineering teams to ensure that the information flow meets the needs of the Automation and Engineering teams, resolving issues as they arise.
What you bring
delta-v
navisworks
initiative
b.sc
communication
gmp
Familiar with Delta-V & Navis Works an advantage.
Demonstrated ability to work on own initiative and proactively respond to business needs.
B.Sc/B.Eng. degree in engineering discipline, with particular emphasis mechanical or process engineering.
Excellent interpersonal and communication skills.
Requires extensive experience from biotechnology or pharmaceutical GMP manufacturing/CQV environment.
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