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Biomedical Engineering Consultant Jobs in Indiana

Mechanical Engineering, Mechanical Engineering Technology, Biomedical Engineering, Bioengineering ... Consulting promotes equal opportunities. We are committed to bringing together people from diverse ...

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Biomedical Engineering Job Category: Scientific/Technology All Job Posting Locations: Warsaw ... consultation with works councils and other employee representative bodies, as may be required ...

Biomedical Engineering Job Category: Scientific/Technology All Job Posting Locations: Warsaw ... consultation with works councils and other employee representative bodies, as may be required ...

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Biomedical Engineering Consultant information

See Indiana salary details

$39K

$90.2K

$133.2K

How much do biomedical engineering consultant jobs pay per year?

As of Aug 31, 2026, the average yearly pay for biomedical engineering consultant in Indiana is $90,215.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,900.00 and $110,400.00 per year, depending on experience, location, and employer.

What does a biomedical engineering consultant do?

A Biomedical Engineering Consultant applies engineering principles to healthcare and medical device challenges, providing expertise on product development, regulatory compliance, and technology implementation. They work with hospitals, research institutions, and medical device companies to improve equipment performance, ensure safety standards, and optimize healthcare solutions. Their role may include evaluating new technologies, troubleshooting medical devices, and advising on FDA or ISO regulations.

What are some typical projects a biomedical engineering consultant works on?

Biomedical Engineering Consultants often engage in a variety of projects such as evaluating medical device designs, assisting with regulatory compliance, or advising on the integration of new technology into clinical settings. They may also work on troubleshooting equipment, optimizing device performance, or leading cross-functional teams to develop bespoke biomedical solutions. Projects can range from short-term assessments to long-term partnerships, providing diverse and dynamic work experiences. This role frequently involves collaborating with clinicians, manufacturers, quality assurance teams, and regulatory authorities to drive successful project outcomes.

What are the key skills and qualifications needed to thrive as a biomedical engineering consultant?

To excel as a Biomedical Engineering Consultant, you need in-depth knowledge of biomedical devices, engineering principles, and healthcare regulations, generally supported by a degree in biomedical engineering or a related field. Familiarity with design and analysis software such as MATLAB, SolidWorks, and regulatory standards like FDA or ISO certifications is often required. Outstanding communication, problem-solving skills, and the ability to manage client relationships are essential soft skills. These competencies allow consultants to bridge technical and clinical needs, ensuring safe, compliant, and effective biomedical solutions for clients.

What are the most commonly searched types of Biomedical Engineering Consultant jobs in Indiana?

The most popular types of Biomedical Engineering Consultant jobs in Indiana are:

What job categories do people searching Biomedical Engineering Consultant jobs in Indiana look for?

The top searched job categories for Biomedical Engineering Consultant jobs in Indiana are:

Infographic showing various Biomedical Engineering Consultant job openings in Indiana as of August 2026, with employment types broken down into 88% Full Time, 7% Part Time, 4% Contract, and 1% Nights. Highlights an 85% Physical, 5% Hybrid, and 10% Remote job distribution, with an average salary of $90,215 per year, or $43.4 per hour.

Development Engineer

Warsaw, IN • On-site

Other

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


Job description

Development Engineer I

📍 Warsaw, IN | Hybrid - 5x on-site/week


About the Role

Join a leading global medical technology company's R&D team to design and develop new orthopedic medical devices — from concept to commercialization. You'll work cross-functionally with surgeons, Manufacturing, Quality, and Regulatory teams to bring innovative arthroplasty products to market for an organization recognized as a market leader in joint replacement technology.


What You'll Do

(With mentorship from senior engineers and oversight from your supervisor)

  • Engage with product users — often orthopedic surgeons — to identify unmet clinical needs and observe device usage in context
  • Translate user needs into design requirements that meet business goals while complying with global regulatory standards
  • Create product designs and author design rationale documenting the basis for design decisions
  • Prepare invention disclosures and support patent documentation
  • Coordinate cross-functional teams to produce and inspect prototypes for design verification and validation
  • Develop production specifications accounting for design for manufacturability (DFM) and inspection requirements
  • Identify and document critical-to-quality features to inform quality control inspection plans
  • Execute design verification/validation activities: tolerance stack-ups, benchtop testing, and simulated OR cadaveric evaluations
  • Author and present design control and risk management documentation for cross-functional approval
  • Support Quality, Sourcing, and Manufacturing teams during design transfer to production


What You Bring

  • B.S. from an ABET-accredited program (or global equivalent) in: Mechanical Engineering, Mechanical Engineering Technology, Biomedical Engineering, Bioengineering, Biomedical/Bioengineering Technology, Aerospace Engineering, or Aeronautical Engineering
  • 1–3 years of relevant experience in product development, mechanical/biomedical engineering, or a related engineering function
  • Familiarity with product development fundamentals: CAD, GD&T, tolerance stack-up analysis, design verification & validation, risk management
  • Exposure to design control processes and NPD (new product development) workflows
  • Strong collaboration skills — you'll work closely with surgeons and multiple internal functions


A plus, not a requirement:

  • Experience in medical devices, orthopedics/arthroplasty, or joint replacement
  • Familiarity with FDA regulations, ISO 13485, or design control documentation
  • Any exposure to surgeon-facing product development


Why choose us

  • An international community bringing together more than 110 different nationalities
  • An environment where trust is central: 70% of our leaders started their careers at the entry level
  • A strong training system with our internal Academy and more than 250 modules available
  • A dynamic work environment that frequently comes together for internal events (afterworks, team buildings, etc.)


Amaris Consulting promotes equal opportunities. We are committed to bringing together people from diverse backgrounds and creating an inclusive work environment. In this regard, we welcome applications from all qualified individuals, regardless of sex, sexual orientation, race, ethnicity, beliefs, age, marital status, disability, or other characteristics.