hirly

Cagents

C&Q Lead Engineer

Limerick

See how you match this job — and similar ones. Free.

Upload your resume and hirly scores it against this role at Cagents first, then against similar open jobs, and shows where you fit and why.

PDF or DOCX, up to 12MB. No sign-up to see your matches.

Get past the screening software and onto a recruiter's desk

hirly rewrites your resume for this job — matching the keywords and skills in the posting, moving your most relevant experience to the top, and writing a cover letter to fit. About 30 seconds.

  • Keywords matched to this posting
  • Fit score before you apply
  • Cover letter included

Matched against 2.3M live jobs from 200,000+ employers in 200+ countries.

Tailor my resume for this job →

hirly's read of this role

Seniority
Lead / management
Country
IE
Work mode
On-site / unstated
First seen by hirly
10 Sept 2026

Derived automatically from the posting. Upload your resume above to see how the role scores against it.

the posting

  • 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).

Original posting on Cagents's site ↗

Want this one?

Upload your resume and hirly rewrites it for this job and writes the cover letter — in about thirty seconds, before you sign up.

Tailor my resume for this job