Eyecare Production Unit Supervisor

Our client, a global healthcare leader is currently recruiting for an Eyecare Production Unit Supervisor to join their growing team in Westport, Co. Mayo.
Responsibilities: As an Eyecare Production Unit Supervisor, you will:
Act as key point of technical contact for aseptic compound transfer, fill finish and printing activitiesManage and execute compounding transfers, filling processes, equipment preparation, and support activities in the Eye Care facility to meet clearly stated operational objectives.Lead, motivate, and guide the manufacturing team to maximize effectiveness by clearly communicating tasks and goals, enabling team members to work efficiently and effectivelyPromote a culture of contamination control and compliance with aseptic best practice.Daily reporting on the status of all operations and support activities. Communicate the departmental goals, to provide cost effective quality compliant products in a safe, effective manner.Liaise with program management, supply chain, technical operations quality and engineering groups to ensure effective planning, scheduling and execution of commercial and clinical manufacturing/filling.Resolve operations/project issues by working with team members, project customers, and others as appropriate.Provides direct interface as a subject matter expert with QA department to interact with HPRA, FDA, applicable health authority and internal audits.Develop direct reports by securing appropriate training, assigning progressively · challenging tasks and managing mid-year and annual reviews.Qualifications: Bachelor's degree or equivalent in an Engineering or Science field.Minimum of 5 years' experience in batch processing, automation, commissioning and validation in an FDA/HPRA regulated industry.A minimum of 1 year direct supervisory experience in a team environmentA working knowledge of safety, quality systems, and current Good Manufacturing Practices as applied to equipment and process steps in area of responsibility is required. Familiarity with pertinent regulatory filings. Proficiency with tech transfer process and familiarity with equipment and facilities validation.For a confidential discussion on the role and the organisation please contact Emma Barry today. ****** 091 706719

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