Production Supervisor

ICDS Recruitment

Limerick

Position: Production Supervisor. Reporting to: Production Manager. Responsibilities: Responsible for raw material receipt, production & shipment of high quality medical devices. Ensure that all Quality system procedures and manufacturing procedures are adhered to in order to produce quality product. Ensure that output targets based on capacity plans are attained. Ensure that a high standard of compliance with GMP is maintained in the manufacturing areas. Ensure that changes to relevant procedures/instructions are relayed to those affected in production. Ensure that training needs of employees in the manufacturing area are constantly reviewed and that required training is given as appropriate. Ensure that all LMS training is up to date within the MBU. Monitor employee performance and carry out performance appraisals with employees. Maintain excellent communication channels with the production & distribution teams and with other departments through regular updates. Work closely with other functions to meet delivery requirements. Work on actions from assigned customer complaints, NCR’s, actions from internal/external audits and CAPA’s and determine root cause. Monitornon conformances and rework to ensure they are kept to a minimum. Highlight vendor issues, process issues, compliance issues to the relevant departments. Participate in Product Transfer and Product Development cross functional teams to ensure production readiness to implement new products into manufacturing, this will involve preparing/reviewing manufacturing instructions and Bills of Materials (BOM’s. Ensure adherence to all environmental, health & safety requirements in accordance with company policy. Act as designee for Production Manager as appropriate. Ensure that s Code of Conduct is considered in all business matters carried out. Qualifications: Formal production/engineering qualification and/or relevant manufacturing experience (medical devices, plastics, etc.) Minimum 5 years previous experience in a supervisory position. Strong communication and inter-personal skills. Knowledge of medical device quality standards ISO13485/FDA practices and GMP or similar regulated industry standards. Good computer skills including knowledge of Microsoft®Office. Excellent organisational and team building skills. High self-motivation. Requirements: Willingness and availability to travel on company business. This job originally appeared on RecruitIreland.com.

2793 days ago