CQV Lead - Life Sciences - Contract
Our partner in Tipperary develops and supplies active ingredients and final formulated products for innovative medicines at its manufacturing and R&D facilities. With over 40 years of operation, the plant exports to over 25 countries worldwide, primarily serving Europe, the USA, and Japan.
CQV Lead Responsibilities:
* Manage a team of C&Q Engineers on high-profile client sites throughout the project lifecycle.
* Identify and define the Commissioning and Qualification strategy for specific projects.
* Review technical documentation from the early design phase to ensure alignment with GMP and CQV requirements.
* Investigate and resolve technical issues with assistance from engineers and/or suppliers.
* Ensure site project execution complies with company guidelines, department procedures, and safety standards.
* Familiarize yourself with Mechanical Completion procedures and Construction scope of work (Walkdown, system acceptance, punch list, and follow-up).
* Schedule preparation and progress reviews.
* 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 Client PMs.
* Coordinate Contractors and Vendors.
* Deliver Final Handover reports to Client users.
About You:
* Previous experience as a Senior/Lead CQV Engineer.
* Delta-V experience is desirable, including running EM's and CM's.