Manufacturing Engineer II at Freudenberg Medical
Spiddal, County Galway, Ireland -
Full Time


Start Date

Immediate

Expiry Date

25 Jul, 25

Salary

0.0

Posted On

26 Apr, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Flexible Approach, Problem Solving, Data Analysis, Statistical Data Analysis, Mechatronics, Manufacturing, Regulatory Requirements

Industry

Mechanical or Industrial Engineering

Description

Working at Freudenberg: “We will wow your world!” This is our promise. As a global technology group, we not only make the world cleaner, healthier and more comfortable, but also offer our 52,000 employees a networked and diverse environment where everyone can thrive individually. Be surprised and experience your own wow moments.
At Freudenberg Medical, we make products that save and improve the lives of people every day, all around the world. We are a global provider for medical device design and manufacturing with more than 2,500 employees. Innovation is at the core of our company, and we are proud of our industry-leading quality, lean manufacturing, and focus on innovation in products and processing technologies. Freudenberg Medical is an exciting place to work with lots of opportunity to learn, develop, and grow your career. Come join us and together we can make a difference in the future of healthcare.
Some of your Benefits
Company Pension
Health Insurance
Flexible Work Models
Personal Development
Diversity & Inclusion
Spiddal, Co. Galway
On-Site
Cambus Teoranta
You support our team as

Responsibilities
  • Solution focused, diagnosing and implementing permanent solutions to manufacturing issues in a structured problem-solving approach. Championing problem solving through appropriate documentation and knowledge sharing.
  • Drive Continuous Improvement by leading the implementation of Lean/Six Sigma manufacturing principles.
  • Work within a highly regulated environment ensuring highest product quality is achieved through robust quality system processes such as GMP, NCR and CAPA etc.
  • Improve the production flow to achieve quality at source, rapid feedback from inspections. Ensuring product specification requirements are met and inspection standards are met through concise standard work.
  • Lead teams in the execution of validation activities.
  • Analyse and Implement innovative improvements in operational performance through key Overall Equipment Effectiveness (OEE) metrics Yield, Uptime and Performance. Increasing capability, capacity and stability of processes, product, equipment and materials.
  • Mechanical Design of jigs and fixtures to meet manufacturing requirements, optimise machine changeover time and improve maintenance.
  • Evaluates in conjunction with EHS new equipment/processes/chemicals for environmental impact.
  • Adhere to Plant Safety requirements and Health & Safety requirements relating to your work, assuming responsibility for those aspects of the OH&S System over which you have control to ensure the health and safety of yourself and others. Be aware of the potential environmental impacts associated with your work and the implications of non-conformance
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