Exciting opportunity for an experienced CQV Lead to join our client, a global leader in healthcare, as they continue to expand and grow due to unprecedented success. As the CQV Lead, you will join the Limerick based team and will play a crucial role in ensuring the efficiency and reliability of the equipment onsite.
Responsibilities for the role will include:
Develop strategies for the site's equipment, including alarm rationalisation, monitoring, and response.
Act as the user representative for the design and operation of all equipment on-site.
Collaborate with development teams to influence storage considerations for manufacturing.
Ensure temperature mapping is integrated into control strategies for product interactions.
Define business processes for temperature-controlled unit interactions and develop related work instructions and procedures.
Assist in FMEAs, safety risk assessments, and hazard assessments.
Collaborate with BPs, procurement, and vendors to develop a preventative maintenance programme for onsite equipment.
Assist with the design of dashboards for monitoring alarms and performance.
Bachelor's or master's degree in engineering or a related discipline.
Minimum of 5 years pharmaceutical industry experience.
A proactive, results-oriented individual with a strong background in biologics/pharmaceuticals and a passion for ensuring that high quality standards are being met.
To discover more about this opportunity, apply now or contact Treasa Prior at HRM on +353 87 3983226 for a confidential discussion.