CQV Engineer
About the Role:
* We are seeking a highly skilled professional to lead Commissioning, Qualification and Validation (CQV) initiatives in pharmaceutical facilities.
* The ideal candidate will possess expertise in executing CQV projects for various systems, including utilities and equipment.
Responsibilities:
* Develop, execute and report on CQV activities for assigned systems, ensuring timely completion of projects.
* Create and review technical documentation to guarantee accuracy and adherence to cGMP regulations.
* Collaborate with cross-functional teams to conduct design reviews and system risk assessments.
* Evaluate vendor documentation for compliance with GxP practices.
* Participate in startup activities of energized equipment when necessary.
* Perform P&ID walkdowns with construction teams prior to handover.
* Assist in investigations of process equipment, utility systems, and control system anomalies.
Requirements:
* A minimum of 4 years of experience in the biotechnology and/or pharmaceutical industry, with a background in CQV or similar roles.
* Proven track record of authoring, reviewing and executing CQV activities for various Facility, Utility and Process Equipment.
* Experience with clean utilities and aseptic processing facilities would be beneficial.
This is an excellent opportunity to work with a leading Biologics/Pharmaceutical organization offering great career progression opportunities. If you are a motivated and detail-oriented individual with a passion for CQV, we encourage you to apply.
About Us: Our client is a renowned provider of pharmaceutical services, with a strong presence in Ireland and Europe. We offer a dynamic and supportive work environment, with opportunities for professional growth and development.