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Medical Device Analyst Jobs (NOW HIRING)

Abbott

Title : Medical Device Tester II Location : Plano, TX Duration : 6 Months 100% Onsite Position ... Strong problem-solving and analytical skills * Experience developing test plans, test cases, and ...

Therakos

Medical Device Service Engineer

Madison, WI

Job Title Medical Device Service Engineer Requisition JR000015824 Medical Device Service Engineer ... Mastery of all Service Technician requirements including Evolve Service Log analysis * Develop in ...

BCforward

Data Acquisition Analyst

Warsaw, IN · On-site

Previous experience as a medical device analyst a plus. Skills: Project Management, MS Office Professional Suite,Proficient in MS Access. Knowledge of JDE, DCS, and MAPICS systems and SQL aplus.

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Medical Device Analyst information

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$31K

$73.3K

$130K

How much do medical device analyst jobs pay per year?

As of Jun 9, 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.

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 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.

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Medical Device Analyst jobs near you
Manufacturing Engineer-Medical Device

Manufacturing Engineer-Medical Device

BioPharma Consulting JAD Group

Houston, TX • On-site

$69K - $89K/yr

Contractor

Posted 27 days ago

Job description

The Manufacturing Engineer Contractor will support the design, validation, implementation, and optimization of manufacturing processes and equipment for ophthalmic medical devices used in cataract and vitreoretinal surgeries. This role is hands-on and highly technical, with a strong focus on equipment validation, statistical process control, and continuous improvement in a regulated medical device manufacturing environment.
Key Responsibilities
  • Lead, execute, document, and manage validation activities (IQ/OQ/PQ) to support the introduction or modification of automated and semi-automated production equipment and processes.
  • Design, develop, validate, and implement manufacturing processes for ophthalmic medical devices.
  • Provide hands-on engineering support for manufacturing equipment before, during, and after release to production.
  • Apply Lean Manufacturing and Six Sigma methodologies to optimize production processes.
  • Implement Continuous Monitoring using Statistical Process Control (SPC) to maintain equipment and processes in a validated state.
  • Perform continuous statistical analysis of Critical Quality Attributes (CQAs) and process indicators to ensure compliance with product specifications (CpK / process capability).
  • Design fixtures and create technical drawings using CAD software (e.g., SolidWorks) to support daily production operations.
  • Develop and maintain standard work instructions and procedures to ensure robust and high-quality manufacturing processes.
  • Promote cross-functional collaboration through clear communication and effective coordination with all departments.

Required Skills & Competencies
  • Medical Device Validation (IQ, OQ, PQ)
  • Statistical Process Control (SPC)
  • Statistical Analysis techniques including:
    • DOE
    • ANOVA
    • Gage R&R
    • T-Test
    • Tolerance Interval Analysis
    • Control Charts
    • Process Capability (CpK)
  • Proficiency with statistical software (Minitab)
  • CAD design experience (SolidWorks or equivalent)
  • Strong technical writing skills
  • Effective public speaking and communication skills

Preferred Skills
  • Manufacturing simulation software experience (FlexSim - preferred, not required)

Requirements
Education & Experience
  • Required:
    • Bachelor's Degree in Engineering or Biomedical Engineering
    • Minimum of 1+ year of professional experience in a Medical Device Manufacturing environment
  • Preferred:
    • Master's Degree in Engineering or Biomedical Engineering

Benefits
  • 12-MONTH CONTRACT

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