I highly recommend working with Natalia both if you are looking for a new role or if you are looking for potential candidates. Natalia worked with me through the recruitment process and always gave brilliant advice. She is one of the best recruiters I’ve ever had the pleasure to work with. I was delighted to receive and accept an offer at the end of the process and can’t wait to get started in my new role. Thanks Natalia!
Manufacturing & Engineering
Production Manager
- TypePermanent
- SalaryNegotiable
- LocationWicklow
- Published27 Feb 2023
- Ref#BBBH12467
- Apply now!
Azon are delighted to be partnering with a global medical device company in their recruitment for a Production Manager. They would report into the Director of Operations and oversee and provide leadership for all the activities of the technical department.
The successful candidate would have an in-depth and thorough knowledge of the industry and have a proven track record in leading a team. They would be involved in ensuring all production activities are efficient and compliant.
Our client are industry leaders in their area and boast an excellent work culture, salary and benefits package.
Responsibilities:
- Ensure the technical production team meet deadlines set out by management.
- Ensure quality in the department is championed and drive product improvement initiatives.
- Implement any training necessary for the team.
- Manage any non-conformance, out-of-specification results, deviation which related to the department and implement necessary changes.
- Owner of department related change controls, CAPAs, PAs, design changes and audit actions.
- Act as production lead in any cross-functional activities.
Requirements:
- BSc/Diploma in life science essential.
- A minimum of 5 years industrial experience in medical devices (preferably IVD industry.
- Experience managing key processes within an ISO13485 certified QMS, specifically production operations, design change, NCMR resolution.
- Ability to build relationships and motivate their team.
- Experience with FDA/HPRA regulatory requirements and audits.
- Experience using lateral flow technology (preferred).
- In-depth knowledge of GMP, GLP and International Standards.
- Quality-focused with an excellent attention to detail.