Boston Scientific Corporation has flagged the Senior Manufacturing Engineer (Perm / Defined Term) Galway job as unavailable. Let’s keep looking.

Do you have a demonstrated ability to successfully support busy production lines? Are you a hands-on engineer with an aptitude for technical problem solving? We are now seeking applications from passionate, self-driven manufacturing engineers. Implement your new ideas and make your mark. Apply Today!

About Natus

We’re the leading manufacturer of medical devices and software for a range of specialities, including new-born care, neurology, sleep, hearing and balance markets. Our mission is to improve patient outcomes in target markets through innovative screening, diagnostic and treatment solutions. Our Irish base in Gort, Co. Galway, manufacture and distribute a range of medical device products used in the diagnosis of human neurological disorders.

“The success of our company depends on our employees. This is where you come in”

Here’s what you can expect:

  • Work Schedule: Onsite at Gort, Ireland
  • Attractive salary package.
  • Health Insurance & Life Assurance cover
  • Educational assistance.
  • Active Sports and Social club.
  • Flexi time
  • Free onsite parking

Essential Duties & Responsibilities: 

  • Prioritizes and develops project plans/budgets and communicates regularly on progress for all work activities to top management.
  • Continually seeks to identify and drive improvements in product performance.
  • Develops and executes validation protocols (e.g. IQ, SV, TMV, MVP, MVR) in compliance with US and EU regulations.
  • Development and validation of manufacturing test methods prior to product/process launch.
  • Research, justify and propose capital equipment and/or processes investments.
  • Determine “make versus buy” decisions changing production methods to increase efficiency and reduce costs.
  • Coordinate with other departments the management of activities to relocate parts or tooling.
  • Conceptualize tooling and manufacturing processes, estimate costs for process design, fabrication, and installations.
  • Develops manufacturing procedures to support transferred manufacturing processes.
  • Reviews and approves documents prepared by sister sites or contractor (e.g. Tool Validation report, Risk Assessments, Change Notes).
  • Gives technical guidance to Associate Engineers, technicians and production employee. Ensure all operations strategies and plans are clearly communicated to Quality and Regulatory management and ensure that best practice is fully built into all project plans.
  • Be a core team member of all manufacturing and distribution strategies and assist the Director of Strategy and Integration with all projects. 
  • Assist team in following and developing procedures, promoting good documentation practices, working on CAPA performance, complaint handling, internal audit, production and process controls and nonconforming product.

Travel Requirements: up to 15% domestic or international travel on a project need basis. Travel is likely to be 1 week per month for the first 9 months and will reduce after this.

Education and/or Experience:

  • Minimum Bachelor's Degree in Electronics/Electrical Engineering or similar. 
  • Minimum of 3 years' manufacturing engineering work experience in a heavily regulated industry, preferably medical device
  • Must have: Exposure to validation process protocols in a heavily regulated environment
  • Understanding of working and maintaining Product Design History File.
  • Excellent organizational and interpersonal skills. You are proactive and a team player; you like to take ownership of projects and run with them. 
  • Demonstrate good approach to problem solving and project management.
  • Experience with the application of statistical theories and methods to resolve production and engineering issues.
  • Previous experience with designing or maintaining or supporting automated equipment and manual assembly lines.
  • Strongly Preferred: Good working knowledge of regulatory expectations and industry practices including industry standards 21 CFR Part 820, ISO13485 and MDD.

Natus Medical Incorporated is an Equal Opportunities Employer

#LI-LM1 #LI-POST #INDNATUS

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Confirmed 23 hours ago. Posted 30+ days ago.

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