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We have a requirement for an experienced CQV Lead for a role based on site in North Dublin

We currently have a requirement for a CQV Lead for a large Bio-Pharma development in North Dublin.
The successful candidate will have several years’ experience working in the pharmaceutical industry and be able to operate in compliance with HPRA, MHRA, FDA and cGMP requirements.
Role & Responsibilities include but are not limited to:

  • Lead and coordinate a commissioning and qualification programme, incorporating utilities, upstream and downstream manufacturing equipment
  • Assist the commissioning manager in the planning and tracking of activities
  • Liaise with the various stakeholders on the commissioning team and the overall project to ensure clear communication between all parties
  • Provide technical process support to the commissioning team throughout the project life cycle
  • Oversee the generation, execution and approval of Commissioning & Qualification documentation
  • Responsibility for direct supervision of vendor engineers and contractors during C&Q activities
  • Use of permit to work system or other safety systems to control commissioning activities
  • Participation in HAZOP and design reviews
  • Deliverables such as technical specifications and vendor turnover documentation

Qualifications & Requirements

  • Third level degree in a relevant discipline
  • Proven level of experience in delivering Commissioning, Qualification & Validation (CQV) activities within the pharmaceutical sector
  • Experience of working in a project environment
  • Hands on attitude
  • Excellent oral and written communication skills in English
  • High level of customer orientation/understanding

Please Note

All CV’s are treated in the strictest confidence.
Recruitment agencies need not apply.

Submit an Application Now

Do you have what it takes ?

CQV Lead - DU1875

Dublin, Ireland

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