2 days ago Be among the first 25 applicants
Longford/Roscommon Ireland
CPL Recruitment are once again assisting our valued client source a experienced
JO-2507-554320
Medical Device
Longford/Roscommon Ireland
CPL Recruitment are once again assisting our valued client source a experienced Production Manager to join their team. This is an exciting opportunity to join a manufacturing site that has undergone major investment and expansion since 2022. You will be working with a very friendly and experienced team that have a wealth of experience in the leadership team.
The Production manager will oversee all molding operations. Establishes standards of performance, measure results, analyze workflow and troubleshoot problems.
Excellent benefits including health care, pension scheme, Shared Value Plan, onsite parking, bike to work scheme, annual leave, which increases with length of service, and relocation assistance.
Get in touch for further information : Deirdre Murphy on 01 614 6178 / 087 180 4358 or deirdre.murphy@cpl.ie
Responsibilities
* Managing the performance of our production facility, including resourcing, manpower, and efficiency.
* Monitoring production data (e.g., downtime, waste, non-conformances) and implementing solutions.
* Lead and Performance Manage your direct report(s).
* Ensure duties are defined, communicated and met by direct reports.
* Review and approve all performance evaluations.
* Proactively participate in the Performance Management process to ensure delivery of own, and the wider team's objectives
* Driving a culture of safety and innovation, ensuring our facility is audit-ready every day
* Liaising with cross-functional teams to maintain and improve customer satisfaction
* Ensure customer requirements are met.
* Review and approve labor management.
* Understand all products and quality specifications of active products.
* Establish and monitor plant performance by creating goals and reviewing tracking metrics.
* Develop and communicate plans to reduce scrap.
* Review and approve all performance evaluations.
* Review and investigate all accident reports.
* Verify compliance with all PM Management activities through our Maximo system.
* Track, monitor and verify accuracy of RM, WIP and FG inventories.
* Ensure fair and consistent treatment of all employees by upholding policies and procedures.
* Implement and uphold The Quality System ISO 13485, ensuring GMP compliance, product quality, and adherence to safety and regulatory standards ISO 14001.
* Ability to drive technical and operational enhancements.
* Drive Lean Manufacturing, Six Sigma, or other process improvement initiatives to enhance productivity.
Requirements
* Min 5 years experience in an Injection Molding Medical Device manufacturing facility preferred or general manufacturing operations in a similar high-volume production role.
* Skills: Strong leadership, organizational, and communication skills. Ability to analyze performance data and present actionable insights. The ability to collaborate with all levels of the business.
* Mindset: A results-driven approach with a knack for problem-solving and continuous improvement. Strong understanding of lean manufacturing principles and techniques.
* Education: BSc in Engineering or equivalent in a related technical discipline. A third-level qualification is desirable, but your experience and passion matter most. Working knowledge of IQMS would be an advantage.
* IQMS experience is a distinct advantage, but not essential, as full training will be provided.
Seniority level
* Seniority level
Mid-Senior level
Employment type
* Employment type
Full-time
Job function
* Job function
Marketing, Public Relations, and Writing/Editing
* Industries
IT Services and IT Consulting
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