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Details

CQV Lead


Reference:SMC3895 Location: Tipperary
Qualification:DegreeExperience:Graduate
Job Type:Fixed Term ContractSalary: Not Disclosed
May be suitable for: Validation Coordinator

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 trouble shooting 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 guideline, 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.
  • Project management principles to coordinate CQV activities and reporting to Company and Clients PM.
  • Contractors and Vendors management and coordination.
  • 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.