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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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How much do medical device analyst jobs pay per year?

As of Jun 29, 2026, the average yearly pay for medical device analyst in the United States is $73,261.00, according to ZipRecruiter salary data. Most workers in this role earn between $52,500.00 and $87,000.00 per year, depending on experience, location, and employer.

What are the typical daily responsibilities of a Medical Device Analyst?

As a Medical Device Analyst, your daily tasks often involve reviewing product data, preparing reports on device performance, and ensuring compliance with regulatory standards. You might also conduct risk assessments, analyze user feedback, and work closely with engineering, quality assurance, and regulatory teams to address product issues and improvements. Your role will involve a balanced mix of independent analysis and cross-functional collaboration. Staying detail-oriented and well-organized is key, as your findings directly contribute to device safety, effectiveness, and ongoing improvement.

Will AI replace medical device sales jobs?

AI is unlikely to fully replace medical device sales jobs, as these roles require relationship-building, technical knowledge, and personalized communication that AI cannot replicate. Instead, AI tools can assist sales professionals by providing data analysis, product information, and customer insights to enhance their effectiveness. Success in this field often depends on interpersonal skills, industry certifications, and understanding customer needs.

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.

Is an analyst a high paying job?

Medical Device Analysts typically earn competitive salaries that can increase with experience, certifications, and specialized skills such as regulatory knowledge or data analysis. While salaries vary by location and employer, the role is generally considered to offer good compensation within the healthcare and medical device industries.

Can you make 7 figures in medical sales?

Medical Device Analysts typically do not earn seven-figure salaries, as high earnings in medical sales usually require extensive experience, a strong network, and success in high-value sales roles. Top medical sales professionals may reach six-figure incomes, but seven-figure earnings are rare and often associated with executive or ownership positions rather than entry- or mid-level analyst roles.

What are the key skills and qualifications needed to thrive in the Medical Device Analyst position, and why are they important?

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 the role of a medical device analyst?

A medical device analyst evaluates and monitors medical devices to ensure safety, compliance, and effectiveness. They review regulatory documentation, analyze device performance data, and collaborate with development teams to improve product quality, often using tools like regulatory databases and quality management systems.
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What cities are hiring for Medical Device Analyst jobs? Cities with the most Medical Device Analyst job openings:
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Medical Device Analyst jobs near you
Infographic showing various Medical Device Analyst job openings in the United States as of June 2026, with employment types broken down into 4% As Needed, 13% Full Time, 82% Part Time, and 1% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $73,261 per year, or $35.2 per hour.
Senior Manager Medical Device Safety, Pharmacovigilance

Senior Manager Medical Device Safety, Pharmacovigilance

Us tech Solutions

Whippany, NJ • On-site

Contractor

Posted yesterday

Key responsibilities

  • Provide content input to project teams for designing, planning, and conducting analyses of safety data for the assessment of medical device safety and performance.

  • Provide content input to post-marketing surveillance program activities including system documentation, planning, and report management.

  • Independently review large data sets and prepare reports for submission to Health Authorities under strict timelines and resolve respective queries regarding product safety.

Job description

Company Description
US Tech Solutions is a global staff augmentation firm providing a wide-range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit our website http://www.ustechsolutions.com/.We are constantly on the lookout for professionals to fulfill the staffing needs of our clients, and we currently have a job opening that may interest you
Job Description
Title: Senior Manager Medical Device Safety, Pharmacovigilance
Duration: 12 Months
Location: Whippany, NJ 07981
Job Description:
The Senior Manager Medical Device Safety (MDS) carries out global Pharmacovigilance (PV) business processes and analyses/trends safety data sets related to complaint handling, regulatory reporting and clinical development for Company medical devices and combination products. The Senior Manager MDS is an expert who provides safety oversight and content contributions to design control, clinical evaluations, vigilance reporting to authorities, trending and post-marketing surveillance for Company Pharmaceutical and Consumer Health medical devices and combination products worldwide.
Position summary:
The incumbent provides counsel as PV medical device subject matter expert to ensure that an effective vigilance, post-marketing surveillance (PMS) and trending systems are implemented and maintained which conforms with global requirements/laws. The Senior Manager MDS works cross-functionally to generate solutions and implement process standards consistent with device industry best practices. The incumbent is a strong problem solver and communicator with a solid understanding of global regulations and standards.
The incumbent will be responsible for the production and accuracy of medical device analysis, interpretation of results and content contributions to PMS and Vigilance activities.
Position duties & responsibilities:
• Provide content input to Project teams for designing, planning and conducting analyses of safety data for the assessment of medical device safety and performance.
• Provide content input to the post-marketing surveillance (PMS) program activities including, PMS system documentation, PMS planning and report management.
• Provide content input, develop and execute PMS trending methodologies, analysis, written contributions and trend report preparations.
• Responsible for monitoring, analyzing and applying trending methodologies to the vigilance data submitted to Health Authorities (e.g MDRs).
• Responsible for the production and accuracy of medical device analysis and interpretation of results.
• Independently review large data sets and prepare reports for submission the Health Authorities under strict timelines and resolved respective queries regarding product safety.
Qualifications
Requirements/Preferences
Education Requirement(s):
• Bachelor's Degree in Engineering, Mathematics or Life-science Discipline with 4 years of professional experience in medical devices or similar sector
Skill & Competency Requirements:
• Strong scientific application of statistical methods used for evaluating complaint trends and establishing thresholds for routine trend reviews (e.g. human factor, malfunction, user interface and user safety)
• Background in medical device trending/signal detection and heavy statistical analysis experience.
• Able to develop and administer management information systems for track and trending.
• Strong analytical and technical skills that include data collection, analysis and required report generation
• Strong communication skills and ability to work both, independently and cross-functionally with Quality, Regulatory, Marketing and other applicable functions within the business
• Working understanding of medical device regulations and industry standards globally specifically 21 CFR 820, 803, ISO 13485, and euMDR 2017/745
Preferences:
The individual should be comfortable working in both office/virtual settings and independently.
Additional Information
All your information will be kept confidential according to EEO guidelines.
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About US Tech Solutions

Sourced by ZipRecruiter

US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions.

Industry

It services

Company size

1,001 - 5,000 Employees

Headquarters location

Jersey City, NJ, US

Year founded

2000

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