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Cqv engineers

Dillon Engineering Services
Cqv engineer
Posted: 17 October
Offer description

Job Title: CQV Engineers – Site / Area / Senior Leadership RolesJob Type:12-Month Contract (Hybrid)Locations:Dublin & CorkContract Length:12 months +Rate:€55 – €90 / hour DOEThe ideal candidateMUST hold a valid working visa or citizenship to work in Ireland.OverviewImmediate Requirements – Multiple CQV Roles AvailableDillon Engineering Services is seekingexperienced CQV Engineersto join high-profile biopharmaceutical projects across Dublin and Cork. We are hiring atmultiple levels– fromCQV Site Engineer (execution level)toCQV Area LeadandSenior CQV Ownerroles.This is a fantastic opportunity to work on large-scale projects with long-term prospects, competitive market rates, and exposure to cutting-edge pharmaceutical facilities.Key ResponsibilitiesDepending on level of appointment, responsibilities may include:Leading and managing a team of CQV Engineers throughout the project lifecycle.Developing and implementing Commissioning & Qualification strategies (VMPs, CMPs, SAT, IQ, OQ).Supporting and driving Design Reviews (DR) and GMP Risk Assessments (FMEA) .Reviewing technical documentation from design through execution to ensure GMP/CQV compliance.Managing Mechanical Completion activities : walkdowns, system acceptance, punch lists, and follow-ups.Coordinating contractors, vendors, and stakeholders while troubleshooting technical issues.Applying project management principles for scheduling, reporting, and delivery of CQV milestones.Delivering final handover reports and ensuring alignment with project standards.For senior roles: providing leadership, mentoring junior staff, and managing overall area delivery.Key RequirementsDegree in Engineering or related discipline.10+ years' experience in commissioning and qualification within pharmaceutical facilities.Proven track record leading CQV teams on large-scale international pharma/biopharma projects.Strong knowledge of ISPE guidelines and ASTM E2500 .Hands-on experience with Design Review, GMP Risk Assessments, and technical documentation.Excellent leadership, communication, and stakeholder management skills.Experience with API reactor processes and/or DeltaV systems is highly desirable.To discuss this role in more detail contactCorné at or for a confidential discussion.

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