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Senior Medical Device Analyst Jobs (NOW HIRING)

Medical Device Coder

Indianapolis, IN · On-site

$18 - $24/hr

Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.

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Senior Mechanical Engineer - Medical Device San Diego, CA (Onsite) 130,000-180,000 DOE Join a ... failure analysis, root-cause investigations, tolerance stack-ups, FEA, and design-for ...

Medical Device Coder

Indianapolis, IN · On-site

$18 - $24/hr

Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.

Medical Device Coder

Carmel, IN · On-site

$18.50 - $24.75/hr

Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.

Medical Device Coder

Carmel, IN

$17.75 - $23.75/hr

Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.

Medical Device Coder

Carmel, IN

$17.75 - $23.75/hr

Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.

Medical Device Coder

Carmel, IN · On-site

$17.75 - $23.75/hr

Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.

Medical Device Coder

Indianapolis, IN

$18 - $24/hr

Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.

Medical Device Coder

Indianapolis, IN · On-site

$18 - $24/hr

Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.

Medical Device Coder

Carmel, IN · On-site

$18.50 - $24.75/hr

Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.

Medical Device Coder

Carmel, IN · On-site

$17.75 - $23.75/hr

Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.

Medical Device Coder

Indianapolis, IN · On-site

$18 - $24/hr

Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.

Medical Device Coder

Carmel, IN

$17.75 - $23.75/hr

Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.

Medical Device Coder

Carmel, IN

$17.75 - $23.75/hr

Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.

Medical Device Coder

Carmel, IN · On-site

$17.75 - $23.75/hr

Ability to use approved AI tools, including ChatGPT Projects and Custom GPTs, to support medical device coding research, HCPCS data analysis, content validation, audit review, and workflow efficiency.

Showing results 41-60

Senior Medical Device Analyst information

See salary details

$53.5K

$109.8K

$142.5K

How much do senior medical device analyst jobs pay per year?

As of Aug 15, 2026, the average yearly pay for senior medical device analyst in the United States is $109,846.00, according to ZipRecruiter salary data. Most workers in this role earn between $90,500.00 and $137,000.00 per year, depending on experience, location, and employer.

What is the difference between Senior Medical Device Analyst vs Medical Device Analyst?

AspectSenior Medical Device AnalystMedical Device Analyst
Required CredentialsBachelor's degree, experience in medical device industry, possibly certificationsBachelor's degree, entry-level experience
Work EnvironmentRegulatory agencies, medical device companies, R&D labsManufacturers, quality assurance, regulatory teams
Employer & Industry UsageUsed in larger organizations for advanced rolesEntry to mid-level roles across the industry
Common Search & ComparisonOften compared for career progressionBase role for medical device industry professionals

The main difference between a Senior Medical Device Analyst and a Medical Device Analyst lies in experience and responsibilities. Senior analysts typically have more industry experience, handle complex projects, and may oversee junior staff. Both roles require relevant credentials and work within similar environments, but the senior position indicates a higher level of expertise and leadership within the medical device industry.

More about Senior Medical Device Analyst jobs

What cities are hiring for Senior Medical Device Analyst jobs?

Cities with the most Senior Medical Device Analyst job openings:

What are the most commonly searched types of Medical Device Analyst jobs?

The most popular types of Medical Device Analyst jobs are:

What states have the most Senior Medical Device Analyst jobs?

States with the most job openings for Senior Medical Device Analyst jobs include:

Infographic showing various Senior Medical Device Analyst job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $109,846 per year, or $52.8 per hour.

Medical Device DHF Engineer

Prophecy Technologies

Indianapolis, IN • On-site

Full-time

Posted 20 days ago


Job description

Role Overview:
This role focuses on supporting Design History File (DHF) activities and comprehensive risk management for medical device development projects. The specialist will be responsible for reviewing, updating, and maintaining critical documentation such as dFMEA, uFMEA, and Preliminary Hazard Analysis (PHA), ensuring compliance with regulatory and quality standards throughout the product lifecycle.
Key Responsibilities:
  • Support and manage Design History File (DHF) activities for medical device projects.
  • Review, update, and maintain Global dFMEA and uFMEA documentation, identifying and mitigating risks.
  • Develop and update Preliminary Hazard Analysis (PHA) in line with risk management procedures.
  • Support the creation and maintenance of product risk management files throughout the development lifecycle.
  • Prepare, review, and update Product Characterization documents, Product Specification Documents (PSD), and Critical-to-Quality (CTQ) documents.
  • Support the development and maintenance of Design Input, Design Output, Verification, and Validation documentation.
  • Ensure robust traceability between user needs, design inputs, risk controls, verification activities, and design outputs.
  • Collaborate cross-functionally with Design, Quality, Regulatory, Manufacturing, and Project Management teams.
  • Participate in design reviews, providing technical input on risk management and DHF compliance.
  • Support engineering change assessments and associated documentation updates.
  • Review engineering documents for completeness, accuracy, and compliance with quality system requirements.
  • Identify documentation gaps and recommend corrective actions.
  • Support audits, inspections, and compliance activities related to design control and risk management documentation.
  • Contribute to continuous improvement initiatives for product development and design control processes.
  • Ensure all deliverables comply with applicable regulatory, quality, and Zimmer Biomet procedures and standards.

Required Skills:
  • Ability to establish document traceability between User Needs, Design Inputs, Design Outputs, Risk Management, Verification, and Validation records within Cockpit Cognition.
  • Experience in supporting DHF gap assessments, document linking, metadata management, and compliance reviews.
  • Familiarity with digital DHF structure, document hierarchy, and traceability matrix development.
  • Knowledge of DHF remediation projects and legacy design documentation migration into Cockpit Cognition.
  • Strong written and verbal communication skills for project plans and inter-departmental collaboration.

Qualifications:
  • Experience in medical device development environments, particularly with Design History File (DHF) and risk management processes.