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Medical Device Risk Management Jobs in Chicago, IL

Risk Management Analyst

Northbrook, IL · On-site

$20.19 - $26/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

We offer a competitive salary with a comprehensive benefits package, including medical, dental ... or Management. The associate will make informed decisions based on Risk evaluation criteria.

Risk Management Analyst

Northbrook, IL · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

We offer a competitive salary with a comprehensive benefits package, including medical, dental ... or Management. The associate will make informed decisions based on Risk evaluation criteria.

Director of Risk Management

Chicago, IL · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

The Director of Risk Management will collaborate closely with executive leadership, operational ... Medical, Dental, and Vision Coverage * Prescription Drug Coverage * Health Savings Account (HSA)

Director of Risk Management

Chicago, IL · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

The Director of Risk Management will collaborate closely with executive leadership, operational ... Medical, Dental, and Vision Coverage * Prescription Drug Coverage * Health Savings Account (HSA)

Senior Director, Program Management

Chicago, IL

$119K - $120K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Strong knowledge of medical device product development processes, Design Controls, risk management, and FDA and international regulatory requirements. * Demonstrated ability to proactively identify ...

Medical Device Compliance Specialist

Vernon Hills, IL · Hybrid

$35/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... risk-based documentation, and cross-functional collaboration across Quality, Regulatory Affairs ... manage multiple deadlines in a regulated environment. * Ability to interpret technical product ...

Director of Risk Management

Chicago, IL · On-site

$97.43 - $116.42/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Risk Director will lead incident investigations, manage compliance with regulations, and ... Medical, Dental, and Vision Insurance coverage * Health Savings Account (HSA) and Flexible Spending ...

Director of Risk Management

Chicago, IL · On-site

$97K - $116K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Risk Director will lead incident investigations, manage compliance with regulations, and ... Medical, Dental, and Vision Insurance coverage * Health Savings Account (HSA) and Flexible Spending ...

Director of Risk Management

Chicago, IL · On-site

$97K - $116K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Risk Director will lead incident investigations, manage compliance with regulations, and ... Medical, Dental, and Vision Insurance coverage * Health Savings Account (HSA) and Flexible Spending ...

Director of Risk Management

Chicago, IL · On-site

$150 - $175/hr

POSITION SUMMARY The Director of Risk Management is responsible for the strategic oversight and ... medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or ...

R&D Quality Engineer II

Barrington, IL · On-site

$85K - $105K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Strong understanding of medical device quality systems and risk management principles. * Experience supporting design verification/validation, process validation, and root cause investigations.

Showing results 21-40

Medical Device Risk Management information

See Chicago, IL salary details

$53.1K

$114.9K

$175.1K

How much do medical device risk management jobs pay per year?

As of Aug 15, 2026, the average yearly pay for medical device risk management in Chicago, IL is $114,919.00, according to ZipRecruiter salary data. Most workers in this role earn between $92,700.00 and $132,900.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in medical device risk management, and why are they important?

To thrive in Medical Device Risk Management, you need a solid background in engineering or life sciences, a thorough understanding of regulatory standards (such as ISO 14971), and experience in risk assessment processes. Familiarity with risk management software, quality management systems, and relevant regulatory databases is typically required, along with certifications like Certified Risk Manager (CRM) or RAC. Strong analytical thinking, attention to detail, and effective communication are crucial soft skills for evaluating risks and collaborating with cross-functional teams. These competencies ensure the safety and compliance of medical devices, protecting both end-users and the company from regulatory or safety issues.

What is the difference between Medical Device Risk Management vs Medical Device Quality Assurance?

AspectMedical Device Risk ManagementMedical Device Quality Assurance
Primary FocusIdentifying, evaluating, and mitigating risks associated with medical devicesEnsuring products meet quality standards and regulatory requirements
CertificationsISO 14971, RAPS certifications often preferredISO 13485, regulatory compliance certifications
Work EnvironmentDesign and development teams, risk analysis meetingsManufacturing, inspection, and quality control departments
Industry UsageUsed throughout product lifecycle for safety managementUsed to maintain product quality and compliance

While both roles are essential in the medical device industry, Risk Management focuses on minimizing safety risks throughout the product lifecycle, whereas Quality Assurance ensures products consistently meet quality and regulatory standards. Understanding these differences helps professionals align their skills with industry needs.

What is medical device risk management?

Medical device risk management is the systematic process of identifying, evaluating, and controlling risks associated with medical devices throughout their lifecycle. This process ensures that potential hazards are minimized to protect patient safety and comply with regulatory standards, such as ISO 14971. Risk management includes activities like risk assessment, implementing controls, monitoring, and documenting all steps to demonstrate compliance. It is a critical function in the design, manufacturing, and post-market phases of medical device development.

How does a medical device risk management professional typically collaborate with cross-functional teams during the product development lifecycle?

Medical Device Risk Management professionals work closely with engineering, regulatory affairs, quality assurance, and clinical teams to identify, assess, and mitigate potential risks associated with medical devices. They participate in design reviews, facilitate risk assessments such as FMEA, and ensure that risk controls are effectively implemented and documented according to regulatory standards like ISO 14971. Regular communication and collaboration are essential to align risk management activities with project timelines and compliance requirements, ensuring patient safety and product success.

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

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

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

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

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

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

Infographic showing various Medical Device Risk Management job openings in Chicago, IL as of August 2026, with employment types broken down into 100% Full Time. Highlights an 50% In-person, and 50% Remote job distribution, with an average salary of $114,919 per year, or $55.2 per hour.

Director of Program Management (Medical Device Manufacturing)

Sterling Engineering Inc.

Wheeling, IL

$180K - $205K/yr

Full-time

Re-posted 10 days ago


Job description

Director of Program Management
Greater Chicago Area (relocation available for qualified candidates)
Reports To General Manager
Target Compensation: $180,000-$205,000/year + 20% bonus (up to 40% bonus based on company performance)

Overview
We are seeking a Director of Program Management to lead strategic, client-facing program execution for a high-volume medical device manufacturing operation. This role will serve as the primary executive interface for key customers, ensuring exceptional delivery, long-term partnership growth, and operational excellence.

This leader will oversee cross-functional program management activities across engineering, operations, quality, and supply chain, driving performance from product launch through full-scale production. The ideal candidate brings deep experience in medical device manufacturing, strong business acumen, and a proven ability to lead complex, high-volume programs with a focus on process improvement and customer satisfaction.

Key Responsibilities
  • Serve as the primary executive point of contact for key customers, including Abbott, building strong relationships and ensuring high levels of satisfaction, retention, and growth.
  • Lead and develop a team of Program Managers, ensuring alignment to customer goals, operational priorities, and financial targets.
  • Drive end-to-end program execution across the product lifecycle, from development and launch through high-volume manufacturing and sustaining activities.
  • Partner cross-functionally with Operations, Engineering, Quality, and Supply Chain to ensure seamless program execution and on-time delivery.
  • Establish and monitor key performance indicators (KPIs) for program success, including cost, quality, delivery, and customer satisfaction metrics.
  • Champion process improvement initiatives across program management and operations, with a focus on scalability, efficiency, and margin expansion.
  • Provide strategic direction in customer engagements, including Quarterly Business Reviews, executive updates, and issue resolution.
  • Support business development efforts, including contract negotiations, proposal development, and identification of growth opportunities within existing accounts.
  • Ensure successful transitions of new products into manufacturing, with strong coordination across engineering validation, quality systems, and production readiness.
  • Develop and implement organizational strategies to attract, retain, and develop high-performing program management talent.
Qualifications
  • Bachelor’s degree in Engineering, Business, or a related field required; advanced degree (MBA or MS) preferred.
  • 7+ years (Grade 29) or 9+ years (Grade 30) of progressive experience in program management, operations, or business leadership within medical device manufacturing.
  • Strong experience supporting high-volume manufacturing environments; familiarity with injection molding processes is highly preferred.
  • Demonstrated success managing large, complex customer relationships, ideally with major medical device OEMs such as Abbott.
  • Proven ability to lead cross-functional teams and influence senior internal and external stakeholders.
  • Experience driving process improvement initiatives (Lean, Six Sigma, or equivalent methodologies preferred).
  • Strong financial acumen, including program cost management, forecasting, and margin improvement.
  • Excellent communication, negotiation, and executive presentation skills.
Leadership & Impact
  • Drives the long-term strategic direction and operational success of program management functions.
  • Influences site-level and potentially multi-site performance, including customer satisfaction, revenue growth, and operational efficiency.
  • Acts as a key member of the leadership team, contributing to overall business strategy and execution.