- Operate and/or monitor weigh and dispense activities and support equipment, using
MES/DCS and PLC based systems, to ensure optimum equipment uptime and target
outputs. Equipment will include, yet is not limited to, down flow booth and scales.
- Cleanroom cleaning, housekeeping and materials management in the Weigh and
- Dispense area. Ensure material availability to support operations.
- Pick materials from stored locations in a GMP compliance managed location and transport the materials to the production area in accordance to the SOPs and GMP stated standards of performance.
- To move materials from the production area to the warehouse or any other location within
- the Carlow facility in compliance with the site SOPs and GMP standards.
- To follow direction and instruction regarding the movement of material from delivery vehicles to the Carlow facility and also dispatch of materials from the Carlow Facility.
- To work in a safe manner regarding the lifting and movement of materials.
- Pack out materials and consume to order to simplify processes for IPT (future state).
- To check calibration of equipment ensuring the calibration is up to date. Using the EBR to dispense materials in weigh & dispense.
- Manage equipment flow, including tracking soiled and clean hold times, proper labelling and inventory management of clean and sterile equipment using automated MES system.
- Maintain process equipment, completing preventative maintenance and equipment troubleshooting and repairs where qualified to perform tasks.
- Participate effectively in writing/revising/rolling out accurate operational procedures, training materials for Weigh and Dispense processes and material management; ensure all work is carried out in line with same.
- Support continuous improvement by active participation in investigations and investigation reports, execution/development of change control/QNs, and contribution to projects as appropriate.
- Required to comply with Merck Global Policies, Procedures and Guidelines, regulatory
- requirements and execute current Good manufacturing Practices (cGMP) in the performance of day to day activities and all applicable job functions.
- Work collaboratively to drive a safe and compliant culture in Carlow.
- May be required to perform other duties as business requires.
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