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Freelance Biomedical Chemical Engineering information

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$41K

$94.8K

$140K

How much do freelance biomedical chemical engineering jobs pay per year?

As of Aug 10, 2026, the average yearly pay for freelance biomedical chemical engineering in the United States is $94,807.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,500.00 and $116,000.00 per year, depending on experience, location, and employer.

What is the difference between Freelance Biomedical Chemical Engineering vs Freelance Chemical Engineer?

AspectFreelance Biomedical Chemical EngineeringFreelance Chemical Engineer
CredentialsDegree in biomedical or chemical engineering, certifications in biomedical device designDegree in chemical engineering, process engineering certifications
Work EnvironmentMedical device labs, biotech firms, hospitalsRefineries, manufacturing plants, chemical processing facilities
Industry UsageHealthcare, biotech, medical device industryChemical manufacturing, energy, materials industry

Freelance Biomedical Chemical Engineering focuses on medical and biotech applications, requiring biomedical knowledge, while Freelance Chemical Engineer covers broader chemical processes in industrial settings. Both roles involve engineering expertise but differ in industry focus and work environment.

What cities are hiring for Freelance Biomedical Chemical Engineering jobs? Cities with the most Freelance Biomedical Chemical Engineering job openings:
What are the most commonly searched types of Biomedical Chemical Engineering jobs? The most popular types of Biomedical Chemical Engineering jobs are:
What states have the most Freelance Biomedical Chemical Engineering jobs? States with the most job openings for Freelance Biomedical Chemical Engineering jobs include:
Freelance Biomedical Chemical Engineering jobs near you
Infographic showing various Freelance Biomedical Chemical Engineering job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 83% Full Time, 14% Part Time, 1% Contract, and 1% Summer. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $94,807 per year, or $45.6 per hour.

Product Development Engineer

Sterling Engineering Inc.

North Chicago, IL

$50 - $56/hr

Contractor

Medical, Dental, Vision, Retirement, PTO

Re-posted yesterday

Job description

Job Title: Product Development Engineer (Medical Device)
Location: North Chicago, IL
Hire Type: 12 month contract
Target Pay Rate: $50-$56/hr
Benefits: PTO, paid holidays, BCBS medical plans, dental/vision plans, 401(k), ESOP

Must-Have Skills:
  • Bachelor's degree in Mechanical, Biomedical, Bioengineering, Chemical Engineering, or related engineering discipline
  • 3+ years of medical device, combination product, or pharmaceutical product development experience
  • Experience with Design History Files (DHF) and design controls
  • Experience supporting commercialized/on-market products
  • Strong technical writing, data analysis, and problem-solving skills
  • Experience working with cross-functional teams in a regulated environment
Job Summary:

The Product Development Engineer supports commercially released medical devices and combination products through product lifecycle management, engineering change implementation, supplier change assessments, and manufacturing support. This role partners with cross-functional teams to evaluate, document, test, and implement product changes while ensuring compliance with quality and regulatory requirements.

Job Duties:
  • Support product lifecycle management activities for commercialized medical devices and combination products
  • Evaluate supplier, material, and manufacturing changes to determine product impact
  • Maintain Design History File (DHF) documentation and ensure design traceability
  • Develop and execute verification testing protocols for product and process changes
  • Analyze engineering and test data, investigate deviations, and prepare technical reports
  • Support risk management activities and regulatory compliance initiatives
  • Collaborate with Engineering, Quality, Regulatory, Manufacturing, Supply Chain, and external suppliers to implement product changes
  • Drive continuous improvement initiatives related to engineering processes and documentation
  • Provide technical support for manufacturing and ongoing product performance
Qualifications:
  • Bachelor's degree in Mechanical Engineering, Biomedical Engineering, Bioengineering, Chemical Engineering, or a related technical discipline
  • 3+ years of experience developing or supporting medical devices, combination products, or other regulated products
  • Experience with Design History Files (DHF), design controls, and engineering documentation
  • Knowledge of FDA regulations and medical device quality systems preferred
  • Familiarity with ISO 13485, ISO 14971, ISO 10993, MDR, or similar regulatory standards is a plus
  • Experience with supplier change management is preferred
  • Strong communication, analytical, and problem-solving skills
  • Ability to work independently and collaborate effectively with cross-functional teams
Qualified applicants will receive consideration for employment without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or genetic information.