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Internship Medical Device Analyst Jobs (NOW HIRING)

Advanced Medical Supply

Medical Device Sales Rep

Tampa, FL · On-site

$84K - $114K/yr

We are a diverse and fast growing medical device & equipment company that is committed to focusing ... Develop, analyze, prioritize and execute in order to execute territory plans to achieve business ...

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Internship Medical Device Analyst information

What types of projects can an Internship Medical Device Analyst expect to work on, and how do these projects contribute to the team?

As an Internship Medical Device Analyst, you can expect to work on projects such as market research for emerging technologies, analysis of regulatory requirements, data collection for product testing, and assisting with process documentation. These projects are typically collaborative, allowing interns to work alongside engineers, regulatory specialists, and marketing teams. Your contributions help streamline product development, ensure compliance, and inform strategic decisions, offering valuable exposure to both the technical and business aspects of the medical device industry.

What does an Internship Medical Device Analyst do?

An Internship Medical Device Analyst assists with evaluating medical devices, supporting research, and analyzing data to ensure devices meet regulatory standards and safety requirements. Interns may work alongside engineers and regulatory professionals to help document findings, prepare reports, and participate in testing. This role provides hands-on experience in the medical device industry and helps interns understand the processes involved in bringing a medical device to market.

What is the difference between Internship Medical Device Analyst vs Medical Device Quality Assurance Intern?

AspectInternship Medical Device AnalystMedical Device Quality Assurance Intern
Required CredentialsTypically pursuing or recent graduate in life sciences, engineering, or related fieldsSimilar educational background, often with coursework in quality systems or regulatory affairs
Work EnvironmentHands-on analysis, data review, and supporting product developmentAssisting in quality audits, documentation, and compliance activities
Employer & Industry UsageUsed in medical device companies focusing on product analysis and developmentCommon in companies emphasizing quality management and regulatory compliance

The Internship Medical Device Analyst role focuses on analyzing medical devices, data review, and supporting product development, while the Medical Device Quality Assurance Intern concentrates on quality processes, audits, and compliance. Both roles are entry-level internships requiring similar educational backgrounds and are used within medical device companies but serve different functions within the industry.

What are the key skills and qualifications needed to thrive as an Internship Medical Device Analyst, and why are they important?

To thrive as an Internship Medical Device Analyst, you need a background in biomedical engineering, life sciences, or a related field, along with strong analytical and research skills. Familiarity with data analysis software, regulatory databases, and basic knowledge of FDA or ISO standards is often required. Attention to detail, effective communication, and a collaborative mindset are important soft skills in this role. These competencies are vital to ensure accurate device evaluations, facilitate regulatory compliance, and contribute effectively to cross-functional teams in the medical device industry.
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What are the most commonly searched types of Medical Device Analyst jobs? The most popular types of Medical Device Analyst jobs are:
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Internship Medical Device Analyst jobs near you
Infographic showing various Internship Medical Device Analyst job openings in the United States as of June 2026, with employment types broken down into 99% Full Time, and 1% Part Time. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution.

Med Device Engineer - Contract to Hire

Express Employment Professionals - Edina

Minneapolis, MN • On-site

$35 - $40/hr

Other

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

Job description

A well-established medical device manufacturer in the western Twin Cities is hiring a contract Manufacturing Engineer to support an exciting new-product launch on its production floor. This is a paid, full-time contract (roughly 8 months) with overtime paid at time-and-a-half — a chance to put hands-on, name-brand medical device manufacturing experience on your resume fast. Recent and early-career engineers are strongly encouraged to apply; if you have solid engineering fundamentals and you want to learn quickly in a dynamic, high-impact environment, this role is built for you.

Company does ultimatly want to hire this person on as a fulltime permenent employee.

Why This Role, Why Now

The team is scaling up to support a newly approved, next-generation cardiac device that is rolling out across the U.S. right now. You will be on the floor where these life-changing products are actually built, solving real problems alongside operators and senior engineers. It is a rare window to join a marquee launch at the ground level and grow quickly.

What You'll Do

  • Lead and own manufacturing engineering tasks on the production floor, troubleshooting issues and improving processes and equipment performance.

  • Work shoulder-to-shoulder with operators and technicians — roughly 60% of your time gowned per PPE standards — listening, learning, and solving new issues as they arise.

  • Drive continuous-improvement work: 5S, A3 problem-solving, standard work, waste reduction, and efficiency projects.

  • Collaborate across teams on verification, validation, and technical reviews, considering impacts on related systems and equipment.

What You Bring

  • Bachelor of Science in Engineering (Mechanical, Electrical, Software, or related).

  • 0-4 years of engineering experience — strong new graduates welcome. Internships or any manufacturing exposure are a big plus.

  • Strong analytical and problem-solving skills, and the ability to lead tasks independently and drive results.

  • Excellent communication and collaboration skills, coachability, and comfort interacting with people at all levels.

Preferred

  • Internship or co-op experience in a manufacturing or medical-device environment.

  • Exposure to regulated / ISO manufacturing or cleanroom (gowned) environments.

Schedule & Compensation

  • Full-time contract, ~8 months. Monday–Friday, 1st shift (5:00 AM–3:00 PM); 2nd shift may also be available.

  • Non-exempt — overtime paid at time-and-a-half for hours over 40.