CQV Engineer — Pharma Validation & Commissioning Lead

CAI

Dublin

On-site

EUR 85,000 - 95,000

Full time

14 days+
Application generator

An application made for this job — a tailored resume and cover letter that speak straight to the posting.

Get past ATS filters

Job summary

CAI is seeking experienced Commissioning, Qualification & Validation (CQV) Engineers to support a large scale pharmaceutical manufacturing project in the Netherlands. This role offers the opportunity to work within a multidisciplinary team delivering critical process, utility, and facility qualification activities in a GMP regulated environment.

This is a site-based role with eligibility to work in the EU without visa sponsorship, now or in the future.

Qualifications

  • Previous CQV experience within pharmaceutical, biotech, or life sciences manufacturing environments.
  • Strong understanding of commissioning and qualification methodologies.
  • Experience supporting regulated manufacturing facilities and associated utility systems.
  • Exposure to complex process equipment and containment-focused manufacturing operations is highly desirable.
  • Familiarity with GMP documentation, protocol execution, and project lifecycle delivery.

Responsibilities

  • Execute commissioning and qualification activities for process, utility, and facility systems.
  • Develop, review, and execute qualification documentation in line with project and regulatory requirements.
  • Support system turnover, startup, and operational readiness activities.
  • Liaise with engineering, quality, operations, and project stakeholders to ensure successful project delivery.
  • Participate in walkdowns, punch-list resolution, and troubleshooting activities.
  • Ensure compliance with site quality, safety, and GMP procedures.

Job description

CAI is seeking experienced Commissioning, Qualification & Validation (CQV) Engineers to support a large scale pharmaceutical manufacturing project in the Netherlands. This role offers the opportunity to work within a multidisciplinary team delivering critical process, utility, and facility qualification activities in a GMP regulated environment.

This is a site-based role with eligibility to work in the EU without visa sponsorship, now or in the future.

Get your free, confidential resume review.
or drag and drop your file here.
Similar jobs

Similar jobs worth comparing

CQV Engineer (GMP, Pharma) — EU Site
CQV Engineer (GMP, Pharma) — EU Site

CAI • Dublin

On-site
EUR 65,000 - 90,000
CQV Engineer
CQV Engineer

CAI • Dublin

On-site
EUR 85,000 - 95,000
CQV Engineer – Life Sciences Validation & Commissioning
CQV Engineer – Life Sciences Validation & Commissioning

CAI • Limerick

On-site
EUR 70,000 - 90,000
C&Q Engineer
C&Q Engineer

Hyper Recruitment Solutions Ltd • Waterford

On-site
EUR 60,000 - 80,000
CQV Engineer
CQV Engineer

QCS Staffing • Roscommon

On-site
EUR 65,000 - 90,000
CQV Engineer
CQV Engineer

CAI • Limerick

On-site
EUR 70,000 - 90,000
QA Validation Engineer — CQV in Biotech (Ireland)
QA Validation Engineer — CQV in Biotech (Ireland)

CAI • Limerick

On-site
EUR 65,000 - 90,000
CQV Engineer — GMP & Commissioning Lead (Ireland)
CQV Engineer — GMP & Commissioning Lead (Ireland)

QCS Staffing • Roscommon

On-site
EUR 65,000 - 90,000
On-Site C&Q Engineer - GMP Validation & CAPEX
On-Site C&Q Engineer - GMP Validation & CAPEX

Hyper Recruitment Solutions Ltd • Waterford

On-site
EUR 60,000 - 80,000
QA Validation Engineer — GMP CQV for Biotech & Pharma (Ireland)
QA Validation Engineer — GMP CQV for Biotech & Pharma (Ireland)

CAI • Munster

On-site
EUR 60,000 - 85,000
Competitive salary
Career development