:
1. Support translation of the production plan into executable tasks and allocate to team members as appropriate.
2. Act as Subject Matter Expert and first point of contact to troubleshoot issues and report to advise or advance to team leaders for further investigation or remediation.
3. Role model, train, assess and support the team in GMP, GDocP, EHS, and operational behaviors, ensuring adherence to site, corporate, and regulatory guidelines.
4. Maintain and keep track of equipment condition and readiness for operations, tracking progress and downtime for trending purposes.
5. Be responsible for generation of timely, accurate, and compliant paperwork, electronic records, and system updates. This includes BMR reviews, reconciliations, and MRP transactions.
6. Encourage engagement with continuous improvement initiatives for improving efficiency. Support efforts to make tasks easier and reduce waste or costs.
7. Support the Production Coordinator and act as their deputy when required.
Qualifications/Experience:
8. Experience of working in a pharmaceutical or other regulated environment. Experience of clean room working and knowledge of aseptic manufacturing, filling desirable.
9. Strong proficiency in English and Maths is essential, and a scientific background is required ( A-Levels).
10. Experience of supervision, developing, and training team members.
11. Excellent communication and collaboration skills, with the ability to manage your own workload.
12. Experience in Lean systems and Continuous Improvement (green belt would be desirable).
13. Understanding of pharmaceutical systems controlled by human-machine interfaces.