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Project Engineer Medical Device Jobs in Illinois

ARi

Project Engineer

East Peoria, IL · On-site

Coordinate DUT (Device under Test) modifications, Instrument and Installation of DUT. Execute ... Project Engineer or Test Engineer or Test Lead or related The Benefits of Working at ARi If you ...

Sterling Engineering Inc.

Project Engineer

Waukegan, IL

$75 - $85/hr

Position: Sr Project Engineer / Process Engineer Location: Waukegan, IL 60087 onsite Duration: 24 ... Medical plans to choose from, Dental & Vision plans, 401(k) with a match, and an Employee Stock ...

Intellectt INC

NPI Project Manager

Libertyville, IL · On-site

Lead and manage NPI projects for medical device products. * Coordinate cross-functional teams including Engineering, Quality, Manufacturing, Supply Chain, and Regulatory. * Drive project timelines ...

Saige Partners

Manager, Design Engineering

Huntley, IL · On-site

$140K - $160K/yr

... medical device and healthcare markets. This position plays a critical role in accelerating new ... New Product Commercialization Lead the evolution of the engineering organization toward a project ...

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Showing results 21-40

All JobsProject Engineer Medical Device JobsProject Engineer Medical Device Jobs in Illinois

Project Engineer Medical Device information

See Illinois salary details

$43.6K

$87.8K

$131.8K

How much do project engineer medical device jobs pay per year?

As of Aug 8, 2026, the average yearly pay for project engineer medical device in Illinois is $87,836.00, according to ZipRecruiter salary data. Most workers in this role earn between $71,700.00 and $100,300.00 per year, depending on experience, location, and employer.

What does a project engineer do in the medical device industry?

A Project Engineer in the medical device industry is responsible for planning, coordinating, and managing projects related to the development and manufacturing of medical devices. They oversee project timelines, budgets, and resources, ensuring that all technical and regulatory requirements are met. Their work involves collaborating with cross-functional teams, such as design, quality assurance, and regulatory affairs, to bring safe and effective medical devices to market. Project Engineers also help resolve technical challenges and ensure products comply with industry standards and government regulations.

How does a project engineer in the medical device industry typically collaborate with cross-functional teams during product development?

As a Project Engineer in the medical device field, you’ll work closely with cross-functional teams such as R&D, quality assurance, regulatory affairs, and manufacturing. Collaboration involves coordinating project timelines, ensuring design requirements are met, and facilitating communication between departments to address technical challenges and regulatory compliance. Regular meetings and clear documentation are essential to keep all stakeholders aligned, and you may often serve as a bridge between engineering and non-engineering teams. This collaborative environment fosters innovation and helps ensure the successful and timely launch of safe, effective medical devices.

What is the difference between Project Engineer Medical Device vs Quality Engineer Medical Device?

AspectProject Engineer Medical DeviceQuality Engineer Medical Device
Required CredentialsBachelor's in Engineering, certifications like PMP beneficialBachelor's in Engineering or Science, certifications like CQE preferred
Work EnvironmentDesign, development, and project management teams in manufacturing or R&DQuality assurance, compliance, and inspection teams in manufacturing
Employer & Industry UsageMedical device companies focusing on product development and project executionMedical device companies ensuring product quality and regulatory compliance
Common Search & Comparison IntentUnderstanding project management roles in medical device industryUnderstanding quality assurance roles in medical device industry

The Project Engineer Medical Device focuses on managing product development projects, coordinating teams, and ensuring timely delivery. In contrast, the Quality Engineer Medical Device concentrates on maintaining product quality, compliance with regulations, and conducting inspections. Both roles are essential in medical device companies but serve different functions within the product lifecycle.

What are the key skills and qualifications needed to thrive as a project engineer in the medical device industry?

To excel as a Project Engineer in medical devices, you need a solid background in engineering (typically a degree in biomedical, mechanical, or electrical engineering), experience with product development, and knowledge of regulatory standards like FDA and ISO 13485. Familiarity with CAD software, project management tools, and validation protocols is highly valuable, along with certifications such as PMP or Six Sigma. Strong problem-solving abilities, collaboration, and effective communication are essential soft skills for leading cross-functional teams and resolving technical challenges. These skills and qualifications ensure safe, compliant, and innovative device development that meets patient and market needs.
What are popular job titles related to Project Engineer Medical Device jobs in Illinois? For Project Engineer Medical Device jobs in Illinois, the most frequently searched job titles are:
What job categories do people searching Project Engineer Medical Device jobs in Illinois look for? The top searched job categories for Project Engineer Medical Device jobs in Illinois are:
Project Engineer Medical Device jobs near you
Infographic showing various Project Engineer Medical Device job openings in Illinois as of July 2026, with employment types broken down into 1% As Needed, 75% Full Time, 17% Part Time, 3% Temporary, and 4% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $87,836 per year, or $42.2 per hour.

Contract Medical Device Lead Auditor

DQS

Schaumburg, IL • On-site

Part-time

Re-posted 24 days ago

Job description

Your role
Medical Device Lead Auditor
DQS Inc. has an immediate contract opportunity for a Medical Device Lead Auditor. Working closely with your schedulers, you will visit client locations and perform the audits as specified. Position is home based with extensive travel.
Job Responsibility:
  • Knowledge of principles and methods for management systems audits.
  • Experience with internal, 2nd or 3rd party ISO-9001, ISO 13485, and/ or GMP auditing.
  • Preference given to RAB-QSA or Exemplar Global Lead Auditor or Auditor qualification.
  • Ability to develop an audit scope and audit plan and manage audit team activities.
  • Ability to present the audit team conclusions to the customer and review customer resolution of any nonconformities.
  • Must be able to assess customer needs and meet UL DQS service and customer satisfaction standards.
  • Work independently and project a professional image appropriate to the work environment.
  • Extensive travel.

Your profile
  • Bachelor's degree in a physical or life science or electrical, mechanical or biotechnology engineering required
  • Minimum of four years experience in quality systems management.
  • Minimum of four years experience in medical device development, manufacture and/or testing, with demonstrated knowledge of US, Canada and EU medical device regulatory requirements, experience with device submittals and knowledge of risk management principles such as ISO 14971.
  • Passed or ability to pass an accredited 40-hour ISO 9001 or ISO 13485 lead auditor course.
  • Experience in implementation of ISO 13485, MDD and/ or CMDCAS desired.

EEO is the Law
Right to Work Poster (English)
DQS Inc. is an Equal Opportunity Employer. Minorities/Women/Veterans/Disabled
EQUAL EMPLOYMENT OPPORTUNITY (EEO)
Qualified applicants are considered for employment without regard to race, religion, sex, national origin, age, marital status, sexual orientation, veteran status, disability, or other protected characteristic.
The employer is subject to certain governmental recordkeeping and reporting requirements for the administration of civil rights laws and regulations. In order to comply with these laws, the employer invites employees to voluntarily self-identify their race or ethnicity. Submission of this information is voluntary and refusal to provide it will not subject you to any adverse treatment. The information obtained will be kept confidential and may only be used in accordance with the provisions of applicable laws, executive orders, and regulations, including those that require the information to be summarized and reported to the federal government for civil rights enforcement. When reported, data will not identify any specific individual.
Right to Work Poster (English)
EEO is the Law

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