ZipRecruiter

Log In

1

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

Jobtailor

Research Scientist

Lake Zurich, IL · On-site

$120 - $180/hr

Experience in an FDA-regulated laboratory environment in the drug and medical device industries, including GMP/GLP/GDP operations * Ability to perform analytical laboratory testing and demonstrate ...

New

Viant Medical Inc.

Engineering Manager, NPI

Wheeling, IL · On-site

$135 - $150/hr

Viant is a global medical device partner providing design, development, manufacturing, and assembly ... The NPI Engineering Manager will partner closely with customers, Operations, Quality, Manufacturing ...

New

Viant

Senior Customer Operations Specialist

Wheeling, IL · On-site

$70K - $82K/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 ...

Medical Murray

Quality Technician II

Lake Zurich, IL · On-site

$24 - $36/hr

... a privately owned medical device company specializing in the development, testing, and ... Ability to communicate effectively with Engineering, Quality, and Operations teams. * Good hand-eye ...

Jobtailor

Regulatory Affairs Manager

Lake Forest, IL · On-site

$130 - $170/hr

... Medical Device industry, with a strong focus on managing regulatory operations, developing global regulatory strategies, and ensuring compliance with regulatory agencies. Proven leadership in ...

medplast

Operational Excellence Director

Temple, TX · On-site

About the company: Viant is a global medical device partner providing design, development ... Bachelor's degree in Business, Engineering, Operations Management, or a related field required.

previous pagenext page

Showing results 21-40

All JobsMedical Device Operations JobsMedical Device Operations Jobs in Chicago, IL

Medical Device Operations information

See Chicago, IL salary details

$11

$27

$54

How much do medical device operations jobs pay per hour?

As of Aug 20, 2026, the average hourly pay for medical device operations in Chicago, IL is $27.04, according to ZipRecruiter salary data. Most workers in this role earn between $18.32 and $31.20 per hour, depending on experience, location, and employer.

What is medical device operations?

Medical device operations refer to the processes and activities involved in the manufacturing, assembly, quality control, supply chain management, and distribution of medical devices. This field ensures that devices are produced efficiently, meet regulatory standards, and are delivered safely to healthcare providers and patients. Operations teams collaborate with engineering, quality assurance, and regulatory departments to maintain compliance and optimize production workflows. Their work is crucial for ensuring that medical devices are safe, effective, and readily available for patient care.

What are the key skills and qualifications needed to thrive in medical device operations?

To thrive in Medical Device Operations, you need a solid understanding of regulatory compliance, quality assurance, and supply chain management, often supported by a degree in engineering, life sciences, or business. Familiarity with quality management systems (QMS), FDA regulations, and software like ERP systems is typically required. Strong organizational skills, attention to detail, and effective communication are crucial soft skills for coordinating cross-functional teams and ensuring compliance. These competencies are vital for delivering safe, high-quality medical devices efficiently and in accordance with rigorous industry standards.

What are some common challenges faced by professionals in medical device operations, and how can they be addressed?

Professionals in Medical Device Operations often face challenges related to maintaining strict regulatory compliance, ensuring product quality, and managing cross-functional communication between manufacturing, quality assurance, and regulatory teams. Staying up to date with changing FDA or international regulations is essential, and frequent documentation or process audits can be demanding. Building strong organizational habits, leveraging digital tracking tools, and fostering open communication channels with other departments can help address these challenges and ensure smooth operations.

What is the difference between Medical Device Operations vs Medical Device Quality Assurance?

AspectMedical Device OperationsMedical Device Quality Assurance
Primary FocusManaging manufacturing, supply chain, and product deploymentEnsuring product quality, compliance, and safety standards
Required CertificationsRegulatory knowledge, manufacturing certificationsQuality management certifications, ISO standards
Work EnvironmentManufacturing plants, supply chain settingsQuality labs, compliance departments
Industry UsageUsed across production and logistics teamsUsed within quality control and regulatory teams

Medical Device Operations and Medical Device Quality Assurance roles often overlap but focus on different aspects of the product lifecycle. Operations centers on manufacturing and logistics, while Quality Assurance emphasizes compliance and safety. Both roles require regulatory knowledge and are essential in the medical device industry.

What are the most commonly searched types of Medical Device Operations jobs in Chicago, IL?

The most popular types of Medical Device Operations jobs in Chicago, IL are:

What are popular job titles related to Medical Device Operations jobs in Chicago, IL?

For Medical Device Operations jobs in Chicago, IL, the most frequently searched job titles are:

What job categories do people searching Medical Device Operations jobs in Chicago, IL look for?

The top searched job categories for Medical Device Operations jobs in Chicago, IL are:

What cities near Chicago, IL are hiring for Medical Device Operations jobs?

Cities near Chicago, IL with the most Medical Device Operations job openings:

Medical Device Operations jobs near you
Infographic showing various Medical Device Operations job openings in Chicago, IL as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 89% Physical, 2% Hybrid, and 9% Remote job distribution, with an average salary of $56,234 per year, or $27 per hour.

Research Scientist

Jobtailor

Lake Zurich, IL • On-site

$120 - $180/hr

Other

Posted 2 days ago

New

Job description

  • Conduct drug container and medical device material evaluations studying extractable/leachable compounds that can partition from device materials into infused or transfused fluids
  • Analyze trace organic compounds for medical device materials using chromatography/mass spectrometry
  • Conduct elemental analysis for medical device materials using ICP/MS
  • Independently generate study designs and protocols, and write and distribute final reports
  • Work occasionally with samples including human blood and blood components using procedural controls and personal protective equipment
  • Assist the lab team in managing comprehensive chemical evaluation testing capabilities for medical device materials
  • Support laboratory daily operations, calibrations, and supplies
  • Provide technical input and content for analytical method development and review
  • Operate ICP/MS and chromatography instrumentation with mass spectrometry detection as a technical expert
  • Review laboratory documentation and results produced by colleagues
  • Provide collegial support to fellow scientists
  • Support occupational and environmental safety, compliance obligations, and continuous improvement of ISO 14001 and ISO 45001 management systems
Requirements
  • Working knowledge of laboratory analytical chemistry, including classical techniques and advanced instrument systems
  • 5+ years of experience with modern analytical tools and techniques in medical device and pharmaceutical product development
  • Experience with elemental analysis instrumentation, including ICP/MS
  • Experience with gas chromatography (GC) and liquid chromatography (LC) equipped with mass spectrometry detectors
  • 5+ years of experience with laboratory instrumental techniques, method development, and method validation
  • Experience with instrument system validation desirable
  • Solid experience with analytical mass spectrometry and advanced data processing systems
  • Experience as a study director with accountability for scientific study design, execution, issue resolution, and completion through audit
  • Strong written and verbal communication skills
  • Experience in an FDA-regulated laboratory environment in the drug and medical device industries, including GMP/GLP/GDP operations
  • Ability to perform analytical laboratory testing and demonstrate critical thinking in study design, complex data interpretation, and investigation planning
  • Adequate structural chemistry knowledge to interpret mass spectral data
  • Bachelor’s degree in chemistry required
  • Advanced degree preferred; PhD in chemistry or related discipline preferred
  • Master’s degree in Chemistry with specific relevant experience may be considered
  • Must be authorized to work for any employer in the United States; Fresenius Kabi cannot sponsor or take over sponsorship of an employment visa
  • Must effectively speak, read, write, and understand English
Core Competencies

Demonstrates expertise in analytical chemistry with a focus on drug container and medical device material evaluations, including proficiency in ICP/MS and chromatography techniques. Capable of independent study design, method development, and compliance with FDA regulations in a laboratory environment.

Highest-signal resume keywords
  • ICP/MS Expertise
  • Chromatography Techniques
  • Analytical Method Development
  • FDA-Regulated Laboratory Experience
  • Study Director Accountability
ATS Optimization KeywordsHard Skills
  • Analytical Chemistry
  • Elemental Analysis
  • Gas Chromatography
  • Liquid Chromatography
  • Mass Spectrometry
  • Method Validation
  • Data Processing Systems
  • Study Design
  • Complex Data Interpretation
  • Structural Chemistry Knowledge
Soft Skills
  • Strong Communication Skills
  • Critical Thinking
Certifications & Qualifications
  • Bachelor’s Degree in Chemistry
  • PhD in Chemistry (Preferred)
  • Master’s Degree in Chemistry (Considered)
Industry Keywords
  • Medical Device Development
  • Pharmaceutical Product Development
  • GMP Operations
  • GLP Operations
  • GDP Operations
  • ISO 14001
  • ISO 45001
  • Occupational Safety
  • Environmental Safety
Tools & Technologies
  • Chromatography Instrumentation
  • Mass Spectrometry Detection
  • Laboratory Instrumentation
#J-18808-Ljbffr

Apply