Biomedical Engineering Technician

Indotronix Avani Group

Madison (WI)

On-site

USD 52,000 - 75,000

Full time

6 days ago
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Job summary

Indotronix Avani Group in Madison, WI is seeking a qualified engineer to assemble and test medical device assemblies, final products, and accessories per the manufacturing documentation provided.

Responsibilities include diagnosis, repair, and test equipment maintenance with supervision, ensuring compliance with the quality system and medical device regulations. Strong problem solving and independence are valued.

Qualifications

  • Bachelor’s degree in engineering or related scientific field required.
  • Ability to work independently and motivate staff to meet deadlines.
  • Problem solving and process improvement skills required.

Responsibilities

  • Assemble and test medical device assemblies, final products, and accessories per the manufacturing documentation provided.
  • Perform assembly diagnosis, repair, and test equipment maintenance with supervision.
  • Ensure work is completed in compliance with company quality system and medical device regulations.

Skills

Problem solving
Independent work
Staff motivation

Education

Bachelor’s degree in engineering or related scientific field
Associate’s degree with 2+ years’ experience
High School Diploma with 6+ years of experience

Job description

Assemble and test medical device assemblies, final products, and accessories per the manufacturing documentation provided. Perform assembly diagnosis, repair, and test equipment maintenance with supervision. Ensure work is completed in compliance with company quality system and medical device regulations

Education / Experience / Skills:

  • Bachelor’s degree in engineering or related scientific field. Associate’s degree with 2+ years’ experience or High School Diploma with 6+ years of experience in similar position.
  • Ability to work independently and motivate staff to meet required deadlines.
  • Problem solving and process improvement skills.

Desired Qualifications:

  • Experience working in cGMP setting and controlled documentation
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