Manufacturing Room Supervisor (MANUFRMSUP-TUL1411) Tullamore, Republic of Ireland
- Ensure that all production materials and supplies including documentation are readily available to maintain the batch schedule.
- Completion of Deviations, EERs, CAPAs COs, Risk Assessments and other documentation as required. Perform data trending to support above.
- Identify areas for continuous improvement - Yellow Belts, Process Improvements, 5S, Visual Management.
- Perform batch reviews of LMRs, BMRs etc. Complete data review at source with QA. Ensure documentation is reviewed in a timely manner and returned to QA. Perform any redline of documentation in preparation for updates.
- Run Tier 1 and feed up into Tier 2 (Daily Scrum).
- Organize the area to achieve a satisfactory workflow of activities on time as outlined in the manufacturing schedule.
- Be a safety champion for the area they are responsible for ensuring compliance with EHS guidelines.
- Organize training opportunities within their area to ensure best practices are maintained.
- Ensure area is maintained in GMP audit ready state.
- Support PM of equipment in functional area – perform calibration and maintenance, periodic reviews when required.
- Partipicate in Quality and Safety regulatory audits.