We are seeking a talented and experienced CQV Engineer to join our project team in a leading pharmaceutical company.
About the Role:
* Lead commissioning and qualification activities for state-of-the-art process and packaging equipment, facilities, utilities, and computerized systems.
* Develop, review, and approve cGMP documentation for equipment, facility, utility, and computerized systems validation.
* Drive project success from design through commissioning and qualification phases.
* Manage vendor relationships and ensure compliance with quality standards.
* Spearhead change control initiatives and foster a culture of continuous improvement.
Requirements:
* Bachelor's degree in Engineering, Science, or a related technical field (engineering degree preferred).
* Minimum 5 years of experience in pharmaceutical manufacturing, validation, operations, or engineering.
* Proven validation expertise in Process and Packaging Equipment (OSD), Facilities and Utilities, and Computerized Systems.
* Strong technical writing skills and experience with GMP documentation.
* Proficiency in risk assessment and risk-based approach to validation activities.
* Experience with Electronic Documentation Management Systems (KNEAT, VEEVA, TRACKWISE).
* Excellent problem-solving abilities and innovative thinking.
Benefits:
* A unique opportunity to shape the future of pharmaceutical manufacturing.
* The chance to work on cutting-edge projects and develop your skills.
* A collaborative and dynamic work environment.
How to Apply:
Please apply directly through this advert or contact Kathy Gillen for more information.
Applicants must have a valid work visa for Ireland. We do not offer visa or work permit sponsorship.