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Freelance Medical Device Design Jobs (NOW HIRING)

Senseye

Design Quality Engineer, SaMD

Austin, TX

$100K - $125K/yr

We are looking for a Design Quality Engineer for our software medical device (SaMD) who can partner closely with engineering, clinical, regulatory, and product teams to build practical, audit-ready ...

Imh

Apply knowledge of medical device design and 3D visualization (XR and Spatial Computing) and 3D printing technologies and associated postprocessing techniques and tools, in delivering the Advanced ...

Bracco

Medical Device Assembler I

Eden Prairie, MN · On-site

$18.25 - $22.50/hr

The Medical Device Assembler I is responsible for performing a variety of production tasks related ... design specification requirements * Generate Quality System Records on applicable ACIST/BMT ...

kindeva

Senior Device Engineer

Maryland Heights, MO · On-site

$101K - $138K/yr

Experience in Medical Device or Combination Products Design Controls, Production, Sustaining Engineering role or related field * B.S. Degree in Engineering discipline with 7 - 9 years experience * M.

Bracco

Medical Device Assembler I

Eden Prairie, MN

$18.25 - $22.50/hr

The Medical Device Assembler I is responsible for performing a variety of production tasks related ... design specification requirements * Generate Quality System Records on applicable ACIST/BMT ...

kindeva

Senior Device Engineer

Maryland Heights, MO · On-site

$101K - $138K/yr

Experience in Medical Device or Combination Products Design Controls, Production, Sustaining Engineering role or related field * B.S. Degree in Engineering discipline with 7 - 9 years experience * M.

kindeva

Senior Device Engineer

Maryland Heights, MO · On-site

$101K - $138K/yr

Experience in Medical Device or Combination Products Design Controls, Production, Sustaining Engineering role or related field * B.S. Degree in Engineering discipline with 7 - 9 years experience * M.

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Freelance Medical Device Design information

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How much do freelance medical device design jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for freelance medical device design in the United States is $47.71, according to ZipRecruiter salary data. Most workers in this role earn between $24.28 and $61.78 per hour, depending on experience, location, and employer.

What is freelance medical device design?

Freelance medical device design involves independent professionals or consultants who specialize in creating, developing, and improving medical devices for clients, such as healthcare companies or startups. These freelancers may work on tasks like conceptualization, CAD modeling, prototyping, regulatory documentation, and usability testing. Their expertise helps clients navigate the complex requirements of the medical device industry, including compliance with safety and regulatory standards. By working on a freelance basis, they offer flexible, project-based support without the long-term commitment of hiring full-time staff.

What are some common challenges freelance medical device designers face when managing projects independently?

Freelance medical device designers often encounter challenges such as navigating complex regulatory requirements, managing communication with clients who may have varying levels of technical understanding, and balancing multiple projects with tight deadlines. Additionally, coordinating with external teams, such as manufacturers or clinical experts, can require strong project management and collaboration skills. Staying updated on industry standards and ensuring all design documentation is thorough are also essential to avoid costly revisions or delays.

What are the key skills and qualifications needed to thrive as a freelance medical device designer?

To thrive as a Freelance Medical Device Designer, you need a solid background in biomedical engineering or industrial design, along with knowledge of regulatory standards and prototyping. Proficiency in CAD software (like SolidWorks or AutoCAD), rapid prototyping tools, and familiarity with FDA or CE Mark certification processes is crucial. Strong problem-solving, project management, and client communication skills set top performers apart in this role. These capabilities ensure device safety, regulatory compliance, and successful collaboration with clients and manufacturers in a competitive industry.
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Freelance Medical Device Design jobs near you
Infographic showing various Freelance Medical Device Design 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 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $99,230 per year, or $47.7 per hour.

Sr. Engineer, Device Development

Ocular Therapeutix

Bedford, MA • On-site

$140K - $155K/yr

Full-time

Re-posted 29 days ago

Job description

Ocular Therapeutix, Inc. (NASDAQ:OCUL) is a biopharmaceutical company focused on the formulation, development, and commercialization of innovative therapies for diseases and conditions of the eye using its proprietary bioresorbable hydrogel-based formulation technology, ELUTYX™. Ocular Therapeutix has built a robust product pipeline of drug delivery solutions developed to reduce the complexity and burden of the current standard of care and position itself to become a leader in the ophthalmic space.
Outside of the ophthalmic realm and behind the doors of our headquarters in Bedford, MA, we strive to build a strong culture where employees can flourish and achieve their career goals. We encourage out of the box thinking, cross-functional collaboration, and creativity.
Position Summary:
This position will serve the role of medical device development engineer within Pharmaceutical Development. Experienced engineer who executes technical development of drug delivery medical devices and packaging. The role includes but is not limited to determining design input, generating design outputs, conducting design verification and validation, developing manufacturing and inspection processes, supporting GMP manufacturing of clinical trial material. This individual will execute assigned project activities and work with project team members to develop and manufacture the combination products. They may oversee the execution of project tasks and monitor the activities and deliverables of project aspects in a leadership role. The position is set in a dynamic and fast-paced environment.
Critical areas of focus will be mechanical design, testing, risk management activities, technical transfers, scale-up and new process development.
Principal Duties and Responsibilities include the following:
  • Design medical device mechanical components and packaging.
  • Perform Design Failure Mode and Effects Analysis (DFMEA) and User Failure Mode and Effects Analysis (UFMEA)
  • Lead design verification and validation (V&V), design outputs (drawings, specs), and feasibility assessments, including prototyping and lab testing.
  • Collaborate with Quality, Regulatory, Human Factors, and Manufacturing teams, often managing relationships with external CMOs/suppliers.
  • Author technical documentation to ensure compliance with FDA, EU, and ISO standards
  • Communicate project plans, status updates and progress against milestones to project team members including management
  • Generate technical documents including test protocols and reports documenting product and process knowledge
  • Display a strong understanding of product development and transfer needs of commercial development

Qualification Requirements:
  • Minimum of a bachelor's degree (advanced degree desirable) in Mechanical Engineering, Biomedical Engineering or related discipline
  • 8+ years of experience in medical device design, development and testing
  • Strong knowledge and understanding of medical device design controls and product realization processes.
  • Strong knowledge of ISO 13485, ISO 14971, IEC 62366
  • Experience using 3D modeling software such as SolidWorks or ProEngineer
  • Capital project experience, including authoring User Requirement Specifications for processing equipment, vendor proposal selection, design review and Factory Acceptance Testing
  • Demonstrated ability to apply strong fundamental scientific and engineering skills to evaluate processes and develop practical solutions to technical challenges
  • Use of DoE and associated statistical methods for process and design space optimization
  • Demonstrated written and verbal communication skills
  • Demonstrated data analysis and problem-solving skills
  • High degree of initiative and self-motivation to meaningfully advance multiple tasks and projects
  • Strong interpersonal skills
  • Experience solving ambiguous problems
  • Experience creating technical, written content
  • A hard-working, team-player that is passionate about science and can effectively collaborate in a dynamic, cross-functional matrix environment
  • Geometric Dimensioning and Tolerancing (GD&T) practices
  • Ability to interpret and draft technical drawings and schematics
  • Experience designing and developing mechanical assemblies
  • Strong understanding of mechanical engineering principles and methodologies
  • Experience in plastic part design, extrusion techniques and injection molding
  • Familiarity with best practices for implementing automated systems (e.g. GAMP)
  • Drafting of regulatory submission documents and agency audit experience
  1. Working Conditions:
  • Production Floor - gowning requirements
  • Bending
  • Lifting

Salary Range
$140,000-$155,000 USD
Ocular Therapeutix is an Equal Opportunity Employer and complies with all applicable federal, state, and local laws regarding nondiscrimination. Ocular Therapeutix provides equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, or status as a veteran. For information on how Ocular Therapeutix collects, stores, and utilizes candidate information please see our privacy policy found at https://www.ocutx.com/privacy-policy/. For the Privacy Notice for California Job Applicants, please see CCPA Applicant Notice.

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