Our client, a global healthcare leader is currently recruiting for a Biologics Supervisor to join their growing team in Westport, Co. Mayo. Responsibilities: Act as your team's key point of contact and technical expert.Lead and support your team to deliver compounding, filling, lyophilization, equipment preparation, formulation, buffer preparation and processing activities in the biologics fill-finish facility to meet clearly stated operating objectives.Promote and develop a culture of contamination control and compliance with aseptic best practices.Communicate departmental goals to provide cost-effective quality compliant products in a safe, effective manner.Collaborate with program management, supply chain, technical operations, quality, and engineering groups to ensure effective planning, scheduling and execution of commercial and NPI clinical manufacturing.Resolve operations/project issues with team members, project customers, and others as appropriate.Drive operations excellence and key operations targets, including OEE where applicable.Provide direct interface as a subject matter expert with the QA department to interact with HPRA, FDA and applicable health authorities and internal audits.Qualifications: Bachelor's degree in chemistry, pharmacy, engineering or a related scientific field is required; an advanced degree is preferred.Minimum of 5 years experience in batch processing, automation, commissioning, and/or validation in an FDA/HHPRA-regulated industry.Minimum of 1 year of direct supervisory experience in a team environment.Possess strong technical knowledge and application of concepts, practices, and procedures. Works on problems of complex scope where analysis of situations or data involves multiple competing factors. Exercises judgment and advises the appropriate actions.
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