Exciting opportunities available for experienced to join our client, a leading Life Science company based in their new manufacturing facility in. These positions are available on a fixed term 12 months contract.
1. Conduct various sampling activities to support product manufacturing within a cGMP-compliant environment.
2. Perform dosimetric analysis, execute dose mapping, and maintain equipment in accordance with GLP, GMP, and ISO 11137 standards.
3. Ensure all tasks are performed in compliance with applicable regulatory requirements, company policies, and standard operating procedures (SOPs).
4. Contribute to the design and implementation of the site dosimetry laboratory program.
5. Prepare, revise, and maintain documentation as required.
6. Participate in validation activities related to the dosimetry lab and equipment qualification processes.
7. Review and approve laboratory test results.
8. Support root cause investigations and provide technical input when needed.
9. Respond promptly to unplanned events and out-of-specification results, escalating issues to the Supervisor without delay.
10. Analyze and trend data related to environmental and product monitoring, including the creation and presentation of quarterly and annual reports.
11. Third level Science / Manufacturing or equivalent qualification.
12. Preferred 2 years' work experience in a Manufacturing / Science / Quality or equivalent environment.
13. Electron beam or other sterilisation technologies experience desirable.
14. Knowledge in ISO 11137 desirable.
15. Chemistry/Microbiology/Dosimetry Lab experience desirable.