Engineering Technician I - New Product Development at Cretex Medical Component and Device Technologies

Posted in Other about 2 hours ago.

Location: Brooklyn Park, Minnesota





Job Description:

Overview




About Cretex Medical



Cretex Medical is a leading contract manufacturer of precision components and assemblies for the medical device industry. Our customers view us as a trusted partner in the areas of injection molding, laser processing, metal stamping and device assembly. Learn more at www.cretexmedical.com.



Position summary:


The Engineering Technician I will be responsible for working alongside New Product Development Manufacturing Engineers supporting engineering builds and documentation in a medical device contract manufacturing facility. This person is directly responsible for assembling prototypes, executing test protocols, documenting results, evaluating new manufacturing process instructions, and providing feedback to the engineering and manufacturing teams. This position will also assist with developing and maintaining tooling and fixtures.

Responsibilities




Job Duties and Responsibilities

  • Provide development feedback to the engineering team
  • Diagnose and troubleshoot technical issues, including but not limited to, machining, injection molding, laser processing, stamping, or packaging
  • Assist engineers as they create, modify, and test products and processes
  • Inspect products and processes for flaws and identify areas of improvement
  • Conduct tests and collect data in support of development activities
  • Reads and complies with work instructions, set up sheets, standard work and checklists
  • Perform equipment set-ups as required
  • Support part builds as required
  • Support and comply with the company Quality System, ISO, and medical device requirements
  • Understand customer needs and the core business markets we serve
  • Participate in required company meetings



Qualifications




Job Requirements


  • 1 year of experience in a manufacturing role
  • Knowledge of Good Manufacturing Practices & Quality Systems Regulations
  • Must have good communication and documentation skills
  • Must have problem solving and critical thinking skills
  • Working knowledge of CAD software platforms AutoCAD, SolidWorks, or Pro-E experience is desired.
  • Ability to cross train in other areas of production when required
  • Ability to work in a manufacturing environment




Preferred Knowledge, Skills and Abilities
  • Associate Degree in Engineering
  • CAD / Solidworks Experience
  • Engineering experience
  • Medical product experience


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