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Local International Biomedical Engineer Jobs in Minnesota

Vantive

Principal Engineer

Plymouth, MN · On-site

$104K - $156K/yr

... and international regulations and guidance. * May supervise engineers and/or technicians ... Experience and/or Background * BS in Mechanical, Plastics, Biomedical Engineering or a related ...

Vantive

Principal Engineer

Plymouth, MN · On-site

$104K - $156K/yr

... and international regulations and guidance. * May supervise engineers and/or technicians ... Experience and/or Background * BS in Mechanical, Plastics, Biomedical Engineering or a related ...

Medtronic

Prin. Systems Hardware Engineer

Moundsview, MN · On-site

$131K - $172K/yr

... of biomedical engineering in the research, design, manufacture, and sale of instruments or ... Deep knowledge of international standards (IEC 60601-1, 60601-2, CC 47CF$, ANSI C63.27, etc.

Medtronic

Prin. Systems Hardware Engineer

Moundsview, MN · On-site

$131K - $172K/yr

... of biomedical engineering in the research, design, manufacture, and sale of instruments or ... Deep knowledge of international standards (IEC 60601-1, 60601-2, CC 47CF$, ANSI C63.27, etc.

Medtronic

Prin. Systems Hardware Engineer

Moundsview, MN · On-site

$131K - $172K/yr

... of biomedical engineering in the research, design, manufacture, and sale of instruments or ... Deep knowledge of international standards (IEC 60601-1, 60601-2, CC 47CF$, ANSI C63.27, etc.

Abbott

R&D Engineer II

Saint Paul, MN · On-site

$61K - $122K/yr

Career development with an international company where you can grow the career you dream of ... Bachelor's degree in Mechanical Engineering, Electrical Engineering, Biomedical Engineering ...

New

Abbott

R&D Engineer II

Saint Paul, MN · On-site

$61K - $122K/yr

Career development with an international company where you can grow the career you dream of ... Bachelor's degree in Mechanical Engineering, Electrical Engineering, Biomedical Engineering ...

New

SEDAA

Systems Engineer

Saint Paul, MN

$70K - $85K/yr

*****LOCAL CANDIDATE ONLY OR OPEN TO RELOCATE TO St. Paul, MN *NO C2C CANDIDATES***** Job Code: 47255 ... Experience and Education Requirements: • Bachelor's degree in Electrical Engineering, Biomedical ...

New

Abbott

Design Assurance Engineer II

Minneapolis, MN · On-site

Career development with an international company where you can grow the career you dream of ... Bachelor level degree in Engineering or Technical Field; advanced degree / Biomedical Engineering ...

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Showing results 21-40

All JobsLocal International Biomedical Engineer JobsLocal International Biomedical Engineer Jobs in Minnesota

Local International Biomedical Engineer information

What is the difference between Local International Biomedical Engineer vs Clinical Biomedical Engineer?

AspectLocal International Biomedical EngineerClinical Biomedical Engineer
CredentialsBiomedical engineering degree, certifications like CBET or BIOMEDEBiomedical engineering degree, certifications like CBET or BIOMEDE
Work EnvironmentHospitals, clinics, medical device companies, international settingsHospitals, healthcare facilities, medical device maintenance
Employer & IndustryGlobal medical device firms, healthcare organizations, international agenciesHospitals, healthcare providers, medical equipment companies

The Local International Biomedical Engineer typically works across various countries or regions, focusing on international standards and diverse healthcare environments. In contrast, the Clinical Biomedical Engineer primarily operates within local hospitals or clinics, maintaining and troubleshooting medical equipment on-site. Both roles require similar credentials but differ mainly in scope and work setting.

What are the most commonly searched types of International Biomedical Engineer jobs in Minnesota?

The most popular types of International Biomedical Engineer jobs in Minnesota are:

Local International Biomedical Engineer jobs near you

Medical Device Complaint Specialist

Three Point Solutions

Moundsview, MN • On-site

$25 - $27/hr

Contractor

Re-posted 17 days ago

Job description

Job Title:         Medical Device Complaint Specialist

Client:              Medical Device Manufacturing Company

Duration:         2 Years (Possible Extension)

Location:         Mounds View, MN 55112

Shift:                1st Shift

Key Responsibilities

  • Review and evaluate product complaints and adverse event reports.
  • Determine Medical Device Reporting (MDR) and Vigilance reporting eligibility.
  • Prepare and submit MDR, Vigilance Reports (VR), and Adverse Drug Experience (ADE) reports.
  • Monitor complaint investigations through closure and ensure timely follow-up.
  • Review product analysis and investigation results.
  • Ensure compliance with FDA and international (OUS) regulatory requirements.
  • Maintain complaint documentation and regulatory records.
  • Analyze clinical and safety data for regulatory reporting.
  • Collaborate with internal teams and external partners to collect complaint information.
  • Support medical device surveillance and post-market vigilance activities.
  • Maintain knowledge of new products, regulations, and reporting requirements.
  • Support continuous improvement of complaint handling and regulatory reporting processes.

Must-Have Requirements

  • Bachelor's Degree in a Science-related field.
  • 1–2 years of experience in Healthcare, Medical Device, Pharmaceutical, Safety, or Clinical Data Evaluation.
  • Strong computer skills (Microsoft Office, SAP, Siebel, Oracle Clinical, or similar systems).
  • Knowledge of complaint handling and adverse event documentation.
  • Strong analytical and problem-solving skills.
  • Excellent written and verbal communication skills.
  • High attention to detail.
  • Ability to work with regulatory documentation and confidential information.

Preferred Qualifications

  • Degree in Nursing, Biology, Pre-Med, Pre-Vet, Biomedical Engineering, or Biomedical Sciences.
  • Clinical or nursing background.
  • Medical Device industry experience.
  • Knowledge of FDA Medical Device Reporting (MDR) requirements.
  • Knowledge of anatomy and physiology.
  • Experience with complaint investigations and post-market surveillance.
  • Experience with regulatory reporting systems.

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