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Recruitment Consultant & Professional Coach (ICF)
The primary purpose of this position is to lead a team of Manufacturing Operators with the support of team leads in a production environment. In addition, drive process/yield improvements to increase operational efficiency.
Responsibilities:
* Responsible for raw material receipt, production & shipment of high quality medical devices within the business.
* 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 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 on actions from assigned customer complaints, NCR’s, actions from internal/external audits and CAPA’s and determine root cause.
* 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).
Ideally you will have:
* Formal production/engineering qualification and/or relevant manufacturing experience (medical devices, plastics, etc.).
* Minimum 5 years previous experience in a supervisory position desirable.
* Strong communication and inter-personal skills.
* Knowledge of medical device quality standards ISO13485/FDA practices and GMP or similar regulated industry standards.
* Excellent organisational and team building skills.
* Willingness and availability to travel on company business.
For more on this contact Regina at HERO 086 0100903 or jobs@hero.ie
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