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Contract Medical Device Testing Jobs in Chicago, IL

DQS

Contract Medical Device Lead Auditor

Schaumburg, IL · On-site

Your role Medical Device Lead Auditor DQS Inc. has an immediate contract opportunity for a Medical ... Minimum of four years experience in medical device development, manufacture and/or testing, with ...

DQS

Contract Medical Device Lead Auditor

Schaumburg, IL · On-site

Your role Medical Device Lead Auditor DQS Inc. has an immediate contract opportunity for a Medical ... Minimum of four years experience in medical device development, manufacture and/or testing, with ...

Nemera

Laboratory Project Specialist

Chicago, IL

... and contract manufacturing. Nemera's manufacturing sites are located in the US, France, Germany ... for medical device products. This individual will serve as a technical expert in device testing ...

New

Nemera

Laboratory Project Specialist

Chicago, IL · On-site

... and contract manufacturing. Nemera's manufacturing sites are located in the US, France, Germany ... for medical device products. This individual will serve as a technical expert in device testing ...

New

Nemera

Laboratory Project Specialist

Chicago, IL

... and contract manufacturing. Nemera's manufacturing sites are located in the US, France, Germany ... for medical device products. This individual will serve as a technical expert in device testing ...

New

Nemera

Laboratory Project Specialist

Chicago, IL · On-site

... and contract manufacturing. Nemera's manufacturing sites are located in the US, France, Germany ... for medical device products. This individual will serve as a technical expert in device testing ...

New

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All JobsContract Medical Device Testing JobsContract Medical Device Testing Jobs in Chicago, IL

Contract Medical Device Testing information

See Chicago, IL salary details

$22

$37

$72

How much do contract medical device testing jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for contract medical device testing in Chicago, IL is $37.83, according to ZipRecruiter salary data. Most workers in this role earn between $25.53 and $47.31 per hour, depending on experience, location, and employer.

What is the difference between Contract Medical Device Testing vs Medical Device Quality Assurance Specialist?

AspectContract Medical Device TestingMedical Device Quality Assurance Specialist
CredentialsTypically requires technical testing certifications, knowledge of testing standardsRequires quality management system certifications, ISO 13485 knowledge
Work EnvironmentLaboratories, testing facilities, controlled environmentsManufacturing sites, quality departments, regulatory offices
Employer & Industry UsageContract testing labs, CROs, medical device companiesMedical device manufacturers, regulatory agencies

Contract Medical Device Testing focuses on performing specific tests to ensure device safety and compliance, often in labs or testing facilities. Medical Device Quality Assurance Specialists oversee quality systems, compliance, and regulatory adherence within manufacturing or corporate settings. While both roles require knowledge of industry standards, testing professionals concentrate on technical testing, whereas QA specialists focus on quality management and regulatory processes.

What are the most commonly searched types of Medical Device Testing jobs in Chicago, IL? The most popular types of Medical Device Testing jobs in Chicago, IL are:
What are popular job titles related to Contract Medical Device Testing jobs in Chicago, IL? For Contract Medical Device Testing jobs in Chicago, IL, the most frequently searched job titles are:
What job categories do people searching Contract Medical Device Testing jobs in Chicago, IL look for? The top searched job categories for Contract Medical Device Testing jobs in Chicago, IL are:
What cities near Chicago, IL are hiring for Contract Medical Device Testing jobs? Cities near Chicago, IL with the most Contract Medical Device Testing job openings:
Contract Medical Device Testing jobs near you

Contract Medical Device Lead Auditor

DQS

Schaumburg, IL • On-site

Part-time

Re-posted 23 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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