:
1. Provide expert subject matter support on environment, health and safety (EHS) related issues;
2. Provide advice and guidance on EHS issues;
3. Monitor site EHS performance, reporting at local and divisional level.
4. Assist in achieving Continual Process Improvement on Site and other Thermo Fisher locations as required;
5. Management of site EHS documentation and recording systems;
6. Audit Departments/Contractors;
7. Manage and co-ordinate the Risk Assessment Programme;
8. Support the Occupational Health Programme;
9. Co-ordinate site EHS Training.
10. Quality: To implement, maintain and advise on EHS matters related to customers within CTD. This will be in accordance with statutory, regulatory and company standards, procedures and systems that are relevant to cGMP Systems in the workplace which may have an EHS related element. Complete investigation reports, corrective actions, change controls, risk assessments and EHS procedures relevant to the cGMP environment.
11. Customer Allegiance: To ensure the availability and reliability/accuracy of all facility reports in order that they can achieve the plans to satisfy customer requirements. This will be achieved through continued monitoring and updating of the FCSMS (Fisher Clinical Services management System).
12. Improvement & Efficiency: To lead, participate and contribute to Practical Process Improvement (PPI) projects that deliver business EHS objectives in a cost-effective manner.
Minimum Requirements/Qualifications:
13. NEBSOH General Certificate in Occupational Health & Safety or equivalent.
14. Relevant Pharmaceutical/cGMP Industry Environmental, Health and Safety experience or equivalent;
15. Previous experience in an EHS role;
16. Knowledge of EHS legislation;
17. Experience in dealing with Local and Regulatory Authorities;
18. Excellent presentational & motivational skills;
19. Ability to establish effective working relationships and is an effective communicator;