Facilities Coordinator I-IV
Industry : Pharmaceutical
Department: Facilities Maintenance
Role Summary:
Administer, coordinate and perform documentation tasks to maintain the required cGMP state of the Facilities CMMS in the Raheen Facility.
Role Responsibilities include, but are not limited to, the following:
• Coordinator for CMMS system -Blue Mountain Regulatory Asset Manager (BMRAM). Assist in the development and management of BMRAM.
• Train new employees to use BMRAM, provide customer service to Raheen site by assisting users of BMRAM to navigate through the database system or troubleshoot problems encountered.
• Create assets (Equipment Code Numbers – ECNs) for all equipment and instrumentation.
• Create and maintain work plans, measurement documents, schedules and work events.
• Review and update CMMS associated SOP’s (Standard Operating Procedures) & WI’s (Work Instructions).
• Maintain facilities documentation and vendor inspection/maintenance reports pertaining to cGMP related equipment and systems. Maintain ECN & vendor files.
• Prepare CMMS KPI’s and reports.
• Follow current good manufacturing practices (cGMPs).
Education and Experience:
• Requires BS/BEng Engineering or related field; will substitute relevant experience for
education. Must have 2+ years’ experience in biopharmaceutical or regulated industry.
Location: Raheen, Limerick
Contraction Duration: 12 months
To apply for this job email your details to enquiries@qaresources.com.