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Medical Device R&D Jobs in Illinois (NOW HIRING)

Prior experience in Field Medical, Medical Affairs, or Clinical R&D. * Strong knowledge of Dermatology or Immunology and clinical research, clinical practice experience preferred. * Willingness and ...

R&D Technician

Schaumburg, IL · On-site

$44K - $52K/yr

Previous experience in medical device or testing laboratories * Previous experience in handling chemicals * Experience with Good Laboratory Practices (GLP) WHY BISCO, INC.? Bisco, Inc. stands out ...

... device industries with a proven, scientific approach to complex trial data and regulatory ... D. in scientific, medical, clinical discipline * Substantial clinical study protocol experience, as ...

R&D Technician

Schaumburg, IL · On-site

$44K - $52K/yr

Previous experience in medical device or testing laboratories * Previous experience in handling chemicals * Experience with Good Laboratory Practices (GLP) WHY BISCO, INC.? Bisco, Inc. stands out ...

R&D Technician

Schaumburg, IL · On-site

$44K - $52K/yr

Previous experience in medical device or testing laboratories * Previous experience in handling chemicals * Experience with Good Laboratory Practices (GLP) WHY BISCO, INC.? Bisco, Inc. stands out ...

*D.R. Horton, Inc., the largest homebuilder in the U.S.,*was founded in 1978 and is a publicly ... Medical, Dental and Vision * 401(K) * Employee Stock Purchase Plan * Flex Spending Accounts * Life ...

Loan Processor

Schaumburg, IL · On-site

$55K - $63K/yr

D.R. Horton, Inc., the largest homebuilder in the U.S. , was founded in 1978 and is a publicly ... Medical, Dental and Vision * 401(K) * Employee Stock Purchase Plan * Flex Spending Accounts * Life ...

R&D Technician

Schaumburg, IL · On-site

$44K - $52K/yr

Previous experience in medical device or testing laboratories * Previous experience in handling chemicals * Experience with Good Laboratory Practices (GLP) WHY BISCO, INC.? Bisco, Inc. stands out ...

Showing results 41-60

Medical Device R D information

What is a medical device R&D?

A Medical Device R&D job involves researching, designing, and developing new medical devices or improving existing ones. Professionals in this role collaborate with engineers, scientists, and regulatory experts to ensure products meet safety, efficacy, and regulatory standards. They conduct feasibility studies, prototyping, and testing to refine device functionality before commercial production. The role requires a strong understanding of engineering principles, biomedical sciences, and regulatory compliance.

What does a medical device R&D do?

Professionals in Medical Device R&D spend their days designing and prototyping new medical devices, conducting experiments to test functionality and safety, and collaborating closely with cross-functional teams such as manufacturing, clinical affairs, and regulatory specialists. They often work on troubleshooting design challenges, documenting progress, and ensuring their work complies with strict regulatory standards. Regular meetings, technical reviews, and hands-on testing in labs are common, making the environment both collaborative and fast-paced. This role is ideal for individuals who enjoy creative problem-solving and have a passion for improving medical technology.

What are the key skills and qualifications needed to thrive in medical device R&D?

To excel in Medical Device R&D, you typically need a degree in biomedical engineering or a related field, strong problem-solving abilities, and knowledge of regulatory standards such as FDA or ISO. Experience with CAD software, rapid prototyping tools, and quality management systems is highly valuable, along with certifications like Six Sigma or PMP for project management. Strong teamwork, attention to detail, and effective communication skills set candidates apart. These competencies are essential to innovate, ensure compliance, and deliver safe, effective medical devices in a highly regulated industry.

What cities in Illinois are hiring for Medical Device R&D jobs?

Cities in Illinois with the most Medical Device R&D job openings:

Infographic showing various Medical Device R&D job openings in Illinois as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 15% Part Time, and 5% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution.

Molding Engineer - Medical Devices

Collabera

North Chicago, IL

Contractor

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 27 days ago


Job description

Company Description

About Collabera:
Established in 1991, Collabera is one of the fastest growing end-to-end information technology services and solutions companies globally. As a half a billion dollar IT company, Collabera's client-centric business model, commitment to service excellence and Global Delivery Model enables its global 2000 and leading mid-market clients to deliver successfully in an increasingly competitive marketplace.
With over 8200 IT professionals globally, Collabera provides value-added onsite, offsite and offshore technology services and solutions to premier corporations. Over the past few years, Collabera has been awarded numerous accolades and Industry recognitions including.
Collabera awarded Best Staffing Company to work for in 2012 by SIA. (hyperlink here)
Collabera listed in GS 100 - recognized for excellence and maturity
Collabera named among the Top 500 Diversity Owned Businesses
Collabera listed in GS 100 & ranked among top 10 service providers
Collabera was ranked:
32 in the Top 100 Large Businesses in the U.S
18 in Top 500 Diversity Owned Businesses in the U.S
3 in the Top 100 Diversity Owned Businesses in New Jersey
3 in the Top 100 Privately-held Businesses in New Jersey
66th on FinTech 100
35th among top private companies in New Jersey
http://www.collabera.com/about_us/accolades.jsp
Collabera recognizes true potential of human capital and provides people the right opportunities for growth and professional excellence. Collabera offers a full range of benefits to its employees including paid vacations, holidays, personal days, Medical, Dental and Vision insurance, 401K retirement savings plan, Life Insurance, Disability Insurance.

Job Description

             The primary responsibility is in plastic co-injection molding process and polymer melt extrusion process, and their mold/tool design to support for existing and new and pipeline device delivery for device-drug combination products. 
             Major responsibility in device plastic molding, co-injection molding and co-extrusion processes with the design of mold/tool from the small scale to the large scale of commercial production by utilizing GMP and ISO standards, and also testing for high volume productions to support biopharmaceutical products.
             Partnering with third party manufacturing (TPM) from the small-scale molding with mold/tool design to scale up for the commercial production in the co-injection/co-extrusion and their mold/tool design for scale up for commercial applications. 
Major Responsibilities:
             Responsible for medical device part co-injection and co-extrusion processes, and their mold/tool design and scientific molding to support processing optimization for high volume injection and extrusion processes
             Responsible for the molding/extrusion process, polymer material and equipment integration to develop process and broaden the process space of co-injection and co-extrusion processes
             Responsible to partner with TPM to design mold/tool and molding/extrusion process with the selected materials and injection and co-injection molding machine for process optimization
             Responsible to work with design engineers to design and develop the part design and conduct the molding trials to optimize the part design, mold/tool design and molding and co-injection process through quality by design to meet the functionality and manufacturability requirements 
Skills Requirements
             Experience in part molding in co-injection and co-extrusion processes with scientific molding approach to broaden the process space to meet part dimension specs and tolerance ranges
             Experience in Moldflow analysis software and with polymer material properties to assess and predict the part quality in terms of part dimension, warpage, and built stress mitigation to optimized the part quality
             Hand-on experience in co-injection and co-extrusion processes and in partnership with TPM for the part develop and manufacture for multiple layers of co-injection and co-extrusion parts
             Hand-on experience in both melt extrusion and injection molding is preferred 
             Experience in polymer, plasticized polymer and thermoplastic elastomer (TPE) co-injection and melt extrusion and their mold/tool design and development for scale up to commercial production
             Experience in system integration of design, materials, process, equipment and assembly for medical device and experience in device functionality testing of components and assembly
             Experience in partnering with third party manufacturing for production to develop the mold/tool and their design trials for part functionality and manufacturability applications.

Qualifications

BS with preferred 5-10 years of experience; Or MS with preferred 3-10 years of experience; Or Ph.D. with preferred 2-8 years of experience in Molding/Extrusion Engineering, Manufacturing Engineering, Material Engineering, Mechanical Engineering, Biomechanical Engineering, or Biomedical Engineering.

Additional Information

All your information will be kept confidential according to EEO guidelines.