C&Q Lead Engineer

CAI

Limerick

On-site

EUR 130,000 - 180,000

Full time

14 days+
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Job summary

CAI is seeking a C&Q Lead in Limerick to direct commissioning, qualification, and startup of utility systems on a regulated biopharma project. You will drive system readiness, ensure GMP/GEP compliance, coordinate with Emerson, Vendors, Utilities, and Regeneron quality/validation, and hand over to operations.

This role also involves mentoring on-site engineers and leading technical decisions. The ideal candidate has 10+ years C&Q experience in pharma manufacturing and a proven track record

Qualifications

  • 10+ years C&Q in regulated biopharma or pharma manufacturing.
  • Led C&Q programs for multi-system, large-scale facilities.
  • Experience coordinating schedules across multiple workstreams and vendors.
  • Strong knowledge of WFI, utilities, and process systems.

Responsibilities

  • Lead and oversee all C&Q activities in active collaboration with the on-site C&Q Lead.
  • Serve as the primary escalation point for troubleshooting and resolution of technical issues.
  • Conduct system walkdowns and readiness reviews; verify systems are ready for commissioning.
  • Ensure activities comply with GEP (pre-GMP) and GMP (qualification) standards.
  • Manage C&Q resources for applicable systems.
  • Coordinate with Emerson, Vendors, Utilities team, and Regeneron quality/validation.
  • Support system handover to operations; ensure issues resolved and systems meet requirements.
  • Provide guidance and mentorship to other C&Q engineers.

Skills

C&Q Leadership
Regulated Biopharma
Project Scheduling
Vendor Coordination
GMP/GEP
ValGenesis (qualification system)

Tools

Emerson Automation
P&IDs
Documentation management
Process control systems

Job description

CAI Overview

Are You Ready?

CAI is a professional services company established in 1996 that has grown year over year to nearly 800 people worldwide. For Life Sciences and Mission Critical industries that need to deliver critical solutions in high-stakes environments, we provide accelerated operational readiness and unparalleled performance at the highest standard through our rigorous approach, field-tested processes, and elite expertise developed over 30 years.

Job Title: C&Q Lead
Location: Limerick
Contract Type: Staff or Contract

The C&Q Lead will be accountable for directing the commissioning, qualification, and start-up (shakedown) of utility systems within a regulated biopharmaceutical project. The successful candidate will drive system readiness, ensure compliance with regulatory standards, and lead the transition from construction completion through to operational handover.

Key Responsibilities
  • Lead and oversee all C&Q activities in active collaboration with the incumbent on-site C&Q Lead.
  • Serve as the primary escalation point for troubleshooting and resolution of technical issues.
  • Conduct system walkdowns and readiness reviews; verify systems are ready for Commissioning commencement.
  • Ensure all activities comply with GEP (pre-GMP) and GMP (qualification) standards throughout.
  • Manage the C&Q resources for applicable systems.
  • Co-ordinate with Emerson Automation, Vendors, Utilities team, and Regeneron quality/validation.
  • Support system handover to operations; ensure all issues resolved and systems meet operational requirements.
  • Provide guidance and mentorship to other C&Q engineers within the team.
Requirements:
  • 10+ years C&Q in a regulated biopharma or pharmaceutical manufacturing environment.
  • Demonstrated track record leading C&Q programmes for multi-system large-scale bioprocess facilities.
  • Experience managing integrated schedule co-ordination across multiple workstreams and vendors.
Technical Skills
  • Strong knowledge of Cleans and Grey utilities/Facilities WFI, Chilled Water Systems, etc.
  • Proficiency in P&IDs, engineering drawings, functional design specifications, and technical documentation.
  • Experience with process control and automation platforms, particularly distributed control systems and PLC-based architectures.
  • Demonstrated understanding of electronic qualification systems (ValGenesis preferred).
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