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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 ...

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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Internship Medical Device Analyst jobs near you
Infographic showing various Internship Medical Device Analyst job openings in the United States as of May 2026, with employment types broken down into 99% Full Time, and 1% Part Time. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution.
Senior Manager Medical Device Safety, Pharmacovigilance

Senior Manager Medical Device Safety, Pharmacovigilance

Us tech Solutions

Whippany, NJ • On-site

Contractor

Posted 11 days ago

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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