This is an exciting opportunity for an experienced to join our client, a leading Life Science company based in their new manufacturing facility in .
This position is on a fixed term 12-month contract.
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.Analyse 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.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 experience desirable.Knowledge in ISO 11137 desirable.Chemistry/Microbiology/Dosimetry Lab experience desirable.