CQV Lead

Exciting Opportunity with a Pharmaceutical Organization

We’re currently recruiting for an exciting opportunity with a Pharmaceutical organization based in Tipperary. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.

Duties

- Manage team of C&Q Engineers on high profile client site throughout the project lifecycle.
- Delta-V experience is desirable, running EM’s and CMs.
- API experience required.
- Strong troubleshooting experience.
- Identify the appropriate Commissioning and Qualification strategy to apply on specific project and define the list of activities required.
- Review and follow-up technical documentation from the early design phase in order to ensure alignment with GMP and CQV requirements.
- Investigate and resolve technical issues with assistance from engineers and/or suppliers.
- Ensure site project execution is undertaken in compliance with company guidelines, department procedures, and safety standards.
- Be familiar with the Mechanical Completion procedure and Construction scope of work (Walkdown, system acceptance, punch list and follow up).
- Schedule preparation and progress review.
- Organize and review daily activities of other CQV Engineers assigned to the project.
- Apply project management principles to coordinate CQV activities and reporting to Company and Clients PM.
- Manage and coordinate Contractors and Vendors.
- Prepare Final Handover reports to the Client users.

If interested in this posting, please feel free to contact Seán McCarthy on +353 (0)87 798 8480 or sean.mccarthy@lifescience.ie for further information.

#J-18808-Ljbffr