C&Q Engineers

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C&Q Engineer overseeing design review, FAT, CQV, and commissioning for a new pharma facility.
17 days ago ago
Expert & Leadership (13+ years), Intermediate (4-7 years), Experienced (8-12 years)
Contractor
Dublin, County Dublin, Ireland
Onsite
Role
What you would be doing
design review
commissioning
fat testing
action tracking
walkdowns
cqv documentation
  • Participate in design document reviews and ensure that quality aspects are included in design.
  • 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.
  • 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.
  • Participate in construction system completion walkdowns.
  • 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.
What you bring
communication
delta-v
navisworks
b.sc
biotech
initiative
  • Excellent interpersonal and communication skills.
  • Familiar with Delta-V & Navis Works an advantage.
  • B.Sc/B.Eng. degree in engineering discipline, with particular emphasis mechanical or process engineering.
  • Requires extensive experience from biotechnology or pharmaceutical GMP manufacturing/CQV environment.
  • Demonstrated ability to work on own initiative and proactively respond to business needs.
Benefits
Information not given or found
Training + Development
Information not given or found
Your recruiter
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