CQV Lead - Life Sciences Position
Our Partner, a renowned manufacturer in Tipperary, develops and supplies innovative medicines with its state-of-the-art facilities. With over 40 years of experience, the company exports to 25 countries worldwide, primarily serving Europe, USA, and Japan.
CQV Lead Responsibilities:
* Manage a team of C&Q Engineers on high-profile client sites throughout project lifecycles.
* Develop and implement Commissioning and Qualification strategies tailored to specific projects and define required activities.
* Review and ensure technical documentation aligns with GMP and CQV requirements from the early design phase.
* 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 scopes of work (Walkdown, system acceptance, punch lists, and follow-ups).
* Schedule preparation and progress reviews.
* Organize and review daily activities of assigned CQV Engineers.
* Apply project management principles to coordinate CQV activities and reporting to Company and Client PM.
* Manage 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.
* API experience is required.
This Role Suits A Self-Motivated Individual Who Is Able To Work Independently And As Part Of A Team In A Fast-Paced Environment.