Production Manager
Requisition ID:
-0
Department:
Production Department
Reports To:
Director of Operations / Head of Operations
Direct Reports:
Yes (140 staff)
Location:
Fermoy, County Cork, Ireland
About Sanmina Fermoy:
Our Fermoy facility is FDA registered and certified to ISO *****:**** for the manufacture of high-quality PCBAs, subassemblies and complete devices up to and including Class III medical devices.
We specialize in manufacturing automation, offering services through the entire product lifecycle from new product introduction (NPI), prototyping and process validation to complex volume manufacturing, test, shipping and repair in a state-of-the-art environment.
The facility has a track record of 30 years of outstanding operational performance and customer service backed by a highly experienced workforce.
Objectives of Position
Responsible for manufacturing company products at optimum cost, quality, delivery and customer satisfaction in accordance with a defined schedule.
Responsible for identifying and driving improvements in quality, output and cost across all processes in the Fermoy plant.
Responsibilities
Lead a group of production leads, team leaders and operators (140 personnel) according to established procedures and world-class medical manufacturing practices.
Develop and maintain standards of performance for a high-volume 24 × 7 medical manufacturing operation and monitor compliance against predetermined benchmarks.
Plan production, layout of product lines and staffing levels for proper operation.
Provide positive leadership to a large multi-shift team, interpreting company policy and management directives for all production personnel.
Identify and drive improvements in quality, output and cost across all processes in the Fermoy plant.
Provide accurate and timely information to management as directed by ongoing business needs.
Establish and maintain a high level of employee morale, reducing absenteeism and attrition.
Maintain sound disciplinary procedures in line with company requirements.
Supervise compliance with health and safety, environmental and security procedures.
Continuously improve best-practice manufacturing.
Ensure all manufacturing team members are trained to optimum standards and that regular appraisals and performance management are conducted.
Assure ongoing compliance with quality and industry regulatory requirements, including health and safety legislation.
Qualifications
8+ years of experience managing a large number of personnel in a multi-shift structure, preferably in a world-class medical manufacturing environment.
Third-level qualification in business or technology preferred.
3-5 years of experience in an automated manufacturing process.
5+ years of experience identifying and delivering process improvements using lean manufacturing and Six Sigma methodologies.
Excellent communication, interpersonal, and leadership skills.
5+ years of experience in MRP/production planning (IPICS).
5+ years of experience in MES/data analysis.
Proficiency in Microsoft Office tools.
Other Information
Seniority level:
Mid-Senior level
Employment type:
Full-time
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