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Medical Device Analyst Jobs in Minnesota (NOW HIRING)

DivIHN

Senior Systems Engineer (Medical Device)

Plymouth, MN · On-site

$109K - $149K/yr

Senior Systems Engineer (Medical Device) Duration: 12 Months Location: Plymouth, MN Only W2 ... Demonstrated strong analytical and problem-solving skills * Ability to solve problems, develop ...

Boston Scientific

Business Process Analyst I

Arden Hills, MN · Hybrid

$61K - $82K/yr

The Business Process Analyst I supports Device Tracking Operations by analyzing, documenting, and ... Experience in medical device, healthcare, quality, or regulated industry. * Knowledge of FDA ...

New

Boston Scientific

Business Process Analyst I

Arden Hills, MN · On-site

$64K - $86K/yr

The Business Process Analyst I supports Device Tracking Operations by analyzing, documenting, and ... Experience in medical device, healthcare, quality, or regulated industry. * Knowledge of FDA ...

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Showing results 21-40

All JobsMedical Device Analyst JobsMedical Device Analyst Jobs in Minnesota

Medical Device Analyst information

See Minnesota salary details

$30.4K

$71.8K

$127.3K

How much do medical device analyst jobs pay per year?

As of Sep 5, 2026, the average yearly pay for medical device analyst in Minnesota is $71,753.00, according to ZipRecruiter salary data. Most workers in this role earn between $51,400.00 and $85,200.00 per year, depending on experience, location, and employer.

What does a medical device analyst do?

A Medical Device Analyst evaluates, tests, and ensures compliance of medical devices with industry regulations and safety standards. They analyze data, assess product performance, and collaborate with regulatory teams to meet market requirements. Their role often involves reviewing risk assessments, troubleshooting device issues, and supporting the development of new medical technologies. Strong analytical skills and knowledge of medical regulations, such as FDA and ISO guidelines, are essential.

What are the key skills and qualifications needed to thrive as a medical device analyst?

A Medical Device Analyst requires strong analytical skills, attention to detail, and a background in biomedical engineering or a related field, often supported by a bachelor's degree. Familiarity with regulatory standards (such as FDA or ISO), proficiency with data analysis tools, and experience using quality management systems are typically necessary. Excellent problem-solving abilities, effective communication skills, and collaborative teamwork are valuable soft skills in this role. These competencies ensure accurate evaluation, compliance, and the ability to convey findings clearly, supporting safe and effective medical device development.

What is a medical device analyst?

A medical device analyst evaluates and monitors medical devices to ensure they meet safety, quality, and regulatory standards. They often review device performance data, assist with compliance documentation, and stay updated on industry regulations, typically requiring knowledge of medical regulations and analytical skills.

What are popular job titles related to Medical Device Analyst jobs in Minnesota?

For Medical Device Analyst jobs in Minnesota, the most frequently searched job titles are:

What job categories do people searching Medical Device Analyst jobs in Minnesota look for?

The top searched job categories for Medical Device Analyst jobs in Minnesota are:

What cities in Minnesota are hiring for Medical Device Analyst jobs?

Cities in Minnesota with the most Medical Device Analyst job openings:

Medical Device Analyst jobs near you
Infographic showing various Medical Device Analyst job openings in Minnesota as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 15% Part Time, 7% Contract, and 1% Nights. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $71,753 per year, or $34.5 per hour.

Medical Writer

Three Point Solutions, Inc.

Maple Grove, MN • On-site

Full-time

This job post has expired today. Applications are no longer accepted.

Job description

Job Title: Medical Writer
Client: Medical Device Manufacturing Company
Duration: 12 Months
Location: Maple Grove, MN, 55311
**Mandatory- Must be US Citizen or Green Card Holder Only
Key Words:
  • CER (Clinical Evaluation Review/Report) Writing
  • MDR (Medical Device Regulations)
  • EU (European Union)
  • Literature Review (e.g., PubMed)

Responsibilities:
  • Write and review scientific manuscripts, congress abstracts, and scientific meeting presentations aligned with journal and congress guidelines.
  • Prepare clinical content for study investigator meetings, interim data analyses, and other internal/external meetings related to clinical studies.
  • Create symposia (non-CME), speaker decks, post-meeting slide decks, topical slide decks, and other Professional Education modules as needed.
  • Collaborate extensively with internal medical leadership, clinical research scientists, clinical trial managers, medical affairs managers, statisticians, and other medical writers as part of publication teams.
  • Develop partnerships with study investigators, external authors, and interact externally with journals, conference organizers, and freelance/contract medical writers.
  • Ensure clinical data is represented accurately in published literature, slide sets, and other materials.
  • Lead and organize document production meetings and related activities.
  • Review documents related to clinical evidence for proper evaluation and presentation of data, methodology, and interpretation.

Required Qualifications:
  • Degree in Life Sciences (Advanced degree preferred).
  • Experience in Medical Device or Pharmaceutical Industry with a focus on Medical Writing or Clinical Research.
  • Extensive experience in writing, editing, and submitting publications to journals and congresses.

Preferred Qualifications:
  • 5-7 years of relevant experience.
  • Therapeutic area knowledge in peripheral interventions is desired.
  • Excellent written, analytical, verbal, and communication skills.
  • Ability to manage multiple projects independently and meet deliverables on time.
  • Capable of working effectively in a matrix environment.
  • Ability to develop strategic solutions to significant business issues.
  • Commitment to patient safety and product quality by adhering to the Quality Policy and documented quality processes and procedures.

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