This is an exciting opportunity for an experienced Micro Lab Supervisor to join our client, a leading Life Science company based in their new manufacturing facility in Kilkenny. This position is on a fixed term 12 months contract.

Role Responsibilities:

• Provide support for product and manufacturing operations within a cGMP-regulated environment.
• Supervise, mentor, and develop team members to ensure performance and growth.
• Lead the site’s dosimetry program and ensure it is regularly reviewed and updated.
• Manage all dosimetry lab activities, including coordination with external providers and suppliers.
• Author documentation for dosimetry methods, equipment qualification, and validation, and offer technical feedback.
• Support lab setup and ongoing maintenance of laboratory equipment and supplies.
• Oversee and enhance the laboratory training program, ensuring adherence to safety rules and training compliance.
• Review lab results for data accuracy and ensure timely communication of findings.
• Maintain validation and control of the dosimetry lab in compliance with internal policies, regulations, and ISO11137 standards.
• Offer technical expertise in dosimetric release methods, dose mapping, and dose calibration procedures.
• Lead troubleshooting efforts related to dosimetric release and provide technical support as needed.
• Analyze product quality and process data using statistical tools to identify trends and drive improvements; prepare quarterly and annual reports.
• Collaborate with cross-functional teams such as QA, Manufacturing, Engineering, R&D, Regulatory Affairs, and Purchasing to ensure timely task completion.

Education And Experience

• Third level Science / Manufacturing or equivalent qualification.
• Minimum 4 yrs’ work experience in a Pharma / Med device /Life Science /equivalent environment.
• Electron beam or other sterilisation technologies are desirable.
• Knowledge of ISO 11137 is desirable.
• Chemistry/Microbiology/Dosimetry Lab experience is desirable.

Role Responsibilities:

• Provide support for product and manufacturing operations within a cGMP-regulated environment.
• Supervise, mentor, and develop team members to ensure performance and growth.
• Lead the site’s dosimetry program and ensure it is regularly reviewed and updated.
• Manage all dosimetry lab activities, including coordination with external providers and suppliers.
• Author documentation for dosimetry methods, equipment qualification, and validation, and offer technical feedback.
• Support lab setup and ongoing maintenance of laboratory equipment and supplies.
• Oversee and enhance the laboratory training program, ensuring adherence to safety rules and training compliance.
• Review lab results for data accuracy and ensure timely communication of findings.
• Maintain validation and control of the dosimetry lab in compliance with internal policies, regulations, and ISO11137 standards.
• Offer technical expertise in dosimetric release methods, dose mapping, and dose calibration procedures.
• Lead troubleshooting efforts related to dosimetric release and provide technical support as needed.
• Analyze product quality and process data using statistical tools to identify trends and drive improvements; prepare quarterly and annual reports.
• Collaborate with cross-functional teams such as QA, Manufacturing, Engineering, R&D, Regulatory Affairs, and Purchasing to ensure timely task completion