Nordson Medical , a global leader in Interventional Solutions, Fluid Components, and Surgical Solutions, is seeking an experienced and highly motivated individual to join our team. We are committed to creating a diverse and inclusive workplace, and we are looking for candidates who share that same commitment.

EDUCATION AND EXPERIENCE REQUIREMENTS

• Bachelor’s degree in Mechanical, Plastics or Biomedical Engineering is desired. In lieu of a degree, previous experience in a similar or exact role may be considered.
• 3 – 5 years of medical device design and development experience is desired.

SKILLS AND ABILITIES

• Ability to interact with clients and companies in a professional manner.
• Customer focus with proficient communication skills, written and oral.
• Flexibility, persistence, resourcefulness, a drive to succeed, and an entrepreneurial spirit.
• SolidWorks 3D CAD proficiency.
• Familiarity with Design for Manufacturability and Assembly (DFM / DFA) is desired.
• Experience working within operations / engineering to develop strong manufacturing process instructions and operator training to ensure smooth product transition into the manufacturing environment is desired.
• Familiarity with FDA QSR and ISO 13485 medical device regulations is desired.
• Familiarity with probability and statistics.

SUMMARY OF THE ROLE

As a member of our team, you will have the opportunity to work in a dynamic and collaborative environment, where your ideas and contributions will be valued and respected.
The Manufacturing Engineer participates as a team member in the production / engineering team providing line support and engineering support for commercial product and supporting R&D production introduction.

ESSENTIAL JOB DUTIES AND RESPONSIBILITIES

• Contributes to yield / efficiency improvement projects for production.
• Contributes to execution of process validation activities and test protocols.
• Conducts feasibility studies to improve yields, balance the line and increase outputs.
• Completes / maintains preventative maintenance for the cleanroom
• Complete equipment qualification.
• Support R&D projects in phase as they transition into manufacturing.
• Participate in daily meetings to drive improvement from a yield, output and efficiency perspective
• Ensure standard times are accurate and achievable for each part.
• Drive continuous improvement within the site