About Sanmina Fermoy
Our Fermoy, Ireland, facility is FDA registered and certified to ISO ISO13485:2016 for the manufacture of high-quality PCBAs, subassemblies and complete devices up to and including Class III medical devices.
Sanmina Fermoy's core specialization is manufacturing automation. We provide services for the entire product lifecycle from New Product Introduction (NPI), prototyping and process validation to complex volume manufacturing & test, shipping and repair.
We hire people with a range of skills, experience, and backgrounds to fulfill roles in careers such as engineering, quality and manufacturing to name just a few.
OBJECTIVE OF POSITION:
* Responsible for manufacturing company products at optimum cost, quality, delivery and customer satisfaction in accordance with defined schedule.
* Responsible for identifying & driving improvements in Quality, output and cost across all processes in the Fermoy Plant.
RESPONSIBILITIES:
* Leading a group of Production Leads, Team Leaders and Production Operators
according to established procedures and current world class Medical manufacturing practices.
* Responsible for manufacturing products at optimum
cost, quality, customer satisfaction
and delivery in accordance with defined schedule.
* Establish standards of performance for a hi-vol 24 x 7 medical manufacturing operation and monitor same against predetermined standards.
* Responsible for
Production planning, Product Line layout
and staffing levels for proper operation.
* Provide positive
leadership to a large multi-shift team
, by interpreting company policy and management directives for Production personnel.
* Responsible for identifying & driving 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.
* Maintain sound disciplinary procedures in line with Company requirements.
* Supervise compliance with
Health and Safety, Environmental and Security procedures.
* Continuous improvement in best practice manufacturing.
* Ensure all manufacturing team members are trained to optimum standards.
* Perform regular appraisals of all Production employees in compliance with company procedure and manage under performers.
* Quality:
Assure ongoing compliance with quality and industry regulatory requirements
* Health & Safety:
Ensure compliance with Health & Safety Legislation and Regulations.
REQUIREMENTS:
* 8+ years
experience in the management of large number of personnel in a multi-shift structure,
preferably in a world-class medical manufacturing environment.
* Third Level Qualification is desired (Business / Technical).
* 3- 5 years experience in an
Automated Manufacturing Process.
* 5+ years in i
dentifying & delivering Process Improvements utilising LSS methodologies.
* Excellent communication skills, interpersonal skills.
* Excellent Leadership skills.
* 5 + years experience in MRP / Production Planning (IPICS).
* 5+ years experience in MES / Data Analysis.
* Proficient in Office Tools.