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Medical Device Developer Jobs in Chicago, IL (NOW HIRING)

Viant is a global medical device partner providing design, development, manufacturing, and assembly services through capabilities in materials, plastics, metals, extrusion, and automation. With ...

Engineering Manager, NPI

Wheeling, IL · On-site

$135K - $150K/yr

Viant is a global medical device partner providing design, development, manufacturing, and assembly services through capabilities in materials, plastics, metals, extrusion, and automation. With ...

Engineering Manager, NPI

Wheeling, IL · On-site

$135K - $150K/yr

Viant is a global medical device partner providing design, development, manufacturing, and assembly services through capabilities in materials, plastics, metals, extrusion, and automation. With ...

Viant is a global medical device partner providing design, development, manufacturing, and assembly services through capabilities in materials, plastics, metals, extrusion, and automation. With ...

As a Senior Quality Engineer , you will: * Lead verification, validation and maintenance of host ... Be involved in the medical device software design controls activities, in accordance with the FDA ...

Controls Engineer

Libertyville, IL · On-site

$81K - $105K/yr

Medical Devices Manufacturing We are actively hiring a Controls Engineer for a leading Medical Device Manufacturing client. This is an excellent opportunity for professionals with experience in ...

As a Senior Quality Engineer , you will: * Lead verification, validation and maintenance of host ... Be involved in the medical device software design controls activities, in accordance with the FDA ...

In this hands-on position, you will support engineering and development teams by performing inspections, testing, documentation reviews, and quality activities that help bring new medical device ...

Support processes for Medical Device Reporting and Complaints for Avalign as specification developer products. * Ensure required design documentation is retained in design history files and technical ...

Controls Engineer

Libertyville, IL · On-site

$81K - $105K/yr

Seeking a Controls Engineer with strong experience in PLCs, automation, and SCADA systems to support a high-volume medical device manufacturing plant. The role includes commissioning new equipment ...

Sustaining Project Manager

Buffalo Grove, IL · On-site

$116K/yr

Manage sustaining and post-launch projects for medical device products. * Coordinate with Engineering, Manufacturing, Quality, Supply Chain, and Regulatory teams. * Support product enhancements ...

Controls Engineer

Libertyville, IL · On-site

$81K - $105K/yr

I am reaching out regarding an exciting opportunity for a Controls Engineer position with one of our prestigious medical device clients. We are seeking professionals with experience in Allen Bradley ...

Showing results 41-60

Medical Device Developer information

See Chicago, IL salary details

$51.5K

$100.4K

$154.6K

How much do medical device developer jobs pay per year?

As of Aug 9, 2026, the average yearly pay for medical device developer in Chicago, IL is $100,398.00, according to ZipRecruiter salary data. Most workers in this role earn between $86,600.00 and $110,800.00 per year, depending on experience, location, and employer.

What is the difference between Medical Device Developer vs Medical Device Engineer?

AspectMedical Device DeveloperMedical Device Engineer
CredentialsTypically requires a degree in biomedical engineering, mechanical engineering, or related fields; certifications like Certified Biomedical Equipment Technician (CBET) are commonSimilar credentials; often holds engineering degrees and may have certifications in medical device design or quality assurance
Work EnvironmentResearch labs, product development teams, manufacturing facilitiesDesign, testing, and quality assurance in labs or manufacturing settings
Industry UsageUsed interchangeably in some companies; focuses on product development lifecycleMore technical focus on engineering aspects, testing, and compliance

While both roles require similar educational backgrounds and work environments, Medical Device Developers often focus on the overall product development process, including design and user needs, whereas Medical Device Engineers concentrate on technical design, testing, and ensuring compliance with standards.

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

To thrive as a Medical Device Developer, you need a strong background in biomedical engineering, product design, and regulatory compliance, typically supported by a relevant degree. Familiarity with CAD software, prototyping tools, and knowledge of FDA or ISO regulatory standards is essential. Creative problem-solving, attention to detail, and effective teamwork are crucial soft skills in this field. These abilities ensure that innovative, safe, and compliant medical devices are developed efficiently to improve patient outcomes.

What are some common challenges medical device developers face when working on new product designs?

Medical Device Developers often encounter challenges related to balancing strict regulatory requirements with innovative design. They must ensure products meet safety and efficacy standards set by agencies like the FDA, while also collaborating closely with cross-functional teams such as engineers, clinicians, and quality assurance. Addressing feedback from clinical trials and adapting to evolving technologies can also add complexity to the development process. Successful developers are adaptable, detail-oriented, and proactive in problem-solving to navigate these hurdles efficiently.

What does a medical device developer do?

A Medical Device Developer is responsible for designing, developing, testing, and refining medical devices such as diagnostic equipment, implants, and monitoring tools. They collaborate with engineers, healthcare professionals, and regulatory bodies to ensure products are safe, effective, and compliant with industry standards. The role involves a combination of research, prototyping, validation, and documentation throughout the product life cycle. Medical Device Developers must stay updated on technological advancements and regulatory changes to create innovative and reliable healthcare solutions.
Infographic showing various Medical Device Developer job openings in Chicago, IL as of August 2026, with employment types broken down into 80% Full Time, and 20% Contract. Highlights an 80% In-person, and 20% Hybrid job distribution, with an average salary of $100,398 per year, or $48.3 per hour.

Engineering Manager, NPI

medplast

Wheeling, IL

$135K - $150K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 5 days ago


Job description

About the company:

Viant is a global medical device partner providing design, development, manufacturing, and assembly services through capabilities in materials, plastics, metals, extrusion, and automation. With nearly 6,000 employees across 24 locations worldwide, it delivers high-quality, life-enhancing products with the scale and expertise to bring devices to market efficiently. Learn more at Viant Medical’s website or on LinkedIn.

Benefits:  Eligible for benefits effective date of hire!

  • Medical, dental, and vision benefits
  • Company-paid life insurance and disability benefits
  • Generous Paid time off and 10 paid Holidays
  • 401k Plan with Company Match
  • Tuition Reimbursement
  • Voluntary Universal Life and Long-Term Care
  • Voluntary Legal Plan
  • Pet Insurance
  • Home Ownership Program

 

About the site:

Our Wheeling facility combines precision machining and assembly capabilities to deliver high-quality medical device components and finished products.

 

About the role:

The NPI Engineering Manager will lead and develop the Engineering team with primary responsibility for New Product Introduction (NPI), product industrialization, and process development. This role is accountable for successfully transferring new products from concept and design into production by establishing robust manufacturing processes, validation strategies, and scalable production systems. The NPI Engineering Manager will partner closely with customers, Operations, Quality, Manufacturing, and Supply Chain to ensure new products meet safety, quality, delivery, and cost objectives while supporting long-term business growth. This role will primarily support metal-centric medical device products and manufacturing processes. Additionally, this leader will collaborate with the site leadership team to grow partnerships with new and existing customers by promoting a culture of consistently meeting or exceeding customer expectations through Continuous Improvement, Operational Excellence, and High-Performance Teams.

We offer market competitive compensation. Potential salary range for this role is $135k-$150k.  Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law.

 

What you'll do:

  • Lead NPI activities from concept through commercialization, production launch, and stable handoff to Operations. 
  • Manage engineering resources, project priorities, timelines, and budgets to support customer development programs, business growth initiatives, and manufacturing readiness objectives. 
  • Partner directly with customers and internal teams on Design for Manufacturability (DFM), Design for Assembly (DFA), technical reviews, risk assessments, quoting support, and design transfer activities. 
  • Develop and implement robust manufacturing processes for medical device components and assemblies, with emphasis on metal-centric technologies such as CNC machining, Swiss turning, precision grinding, laser processing, metal forming, finishing, and secondary operations. 
  • Drive process characterization, Design of Experiments, equipment qualification, process development, and validation activities, including IQ, OQ, PQ, and controlled Engineering Studies when supported by approved rationale. 
  • Lead cross-functional teams to execute product launches within established safety, quality, delivery, cost, and budget expectations. 
  • Develop manufacturing readiness plans addressing equipment, tooling, fixtures, gauges, inspection methods, work instructions, capacity, staffing, supply chain, and production controls. 
  • Evaluate and implement new manufacturing technologies, automation solutions, capital equipment, and tooling to support product requirements and future business growth. 
  • Ensure NPI activities comply with Viant Quality System requirements, FDA regulations, ISO standards, customer requirements, and EHS policies. 
  • Apply lean manufacturing, risk management, and project management methodologies to improve engineering execution and accelerate commercialization timelines. 
  • Translate customer and product requirements into scalable manufacturing solutions that deliver capable processes, quality performance, and operational efficiency. 
  • Promote accountability, innovation, collaboration, and continuous learning within the engineering team. 
  • Support team development through coaching, performance reviews, succession planning, and alignment with Viant values and career growth opportunities 

 

Requirements

Education/Certification/Experience: 

  • Bachelor of science degree in Engineering or related discipline, advanced degree preferred
  • 7+ years of engineering experience in a regulated manufacturing environment, preferably within the medical device industry. 
  • 4+ years of demonstrated people leadership, technical leadership, or project leadership, including responsibility for engineering teams and cross-functional programs. 
  • Demonstrated experience leading NPI, product industrialization, process development, design transfer, validation, and commercialization projects. 
  • Experience with metal-centric manufacturing processes and precision component production strongly preferred. 
  • Working knowledge of FDA, ISO, OSHA, and applicable quality-system requirements. 

 

Skills/Competencies

  • Strong leader, clear communicator, and highly organized project manager with the ability to manage multiple customer programs and competing priorities. 
  • Excellent interpersonal, conflict-resolution, team-building, and influencing skills across technical, operational, and customer-facing environments. 
  • Strong understanding of design transfer, manufacturing process development, process validation, product commercialization, and production ramp-up within a regulated Quality Management System.. 
  • Strong understanding of FDA and ISO requirements applicable to medical device development and manufacturing. 
  • Demonstrated track record of creative problem solving, risk reduction, and successful product launches. 
  • Direct experience with process characterization, Design of Experiments, capability analysis, and statistical methods, including t-tests, ANOVA, and significance testing. 
  • Expertise in technical documentation, including engineering reports, risk assessments, protocols, IQ/OQ/PQ documentation, Engineering Studies, SOPs, and work instructions. 
  • Advanced proficiency with Microsoft Office, Excel, and Minitab. 
  • Lean Six Sigma Green Belt preferred; Black Belt certification is a plus. 

Viant provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, marital status, amnesty, or status as a covered veteran in accordance with applicable federal, state, and local laws. Viant complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities.