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Medical Device Data Analyst Jobs in Chicago, IL (NOW HIRING)

... days, Medical, Dental and Vision insurance, 401K retirement savings plan, Life Insurance ... Participate in project planning, design reviews and risk assessments using formal risk analysis ...

The Data Analyst will be involved in the programming, data mining and analysis of clinical ... Full Health Benefits (Medical , Dental , Vision, Disability, Life Insurance. ) * 403B Retirement ...

New

Medical Device Integration Specialist- Chicago, IL Salary: $90,000- $100,000/yr Other Forms of ... data-driven strategies that help hospitals improve uptime, simplify oversight, and make more ...

Medical, dental, and vision insurance * Paid holidays and generous paid time off * Retirement ... Mentorship from experienced data professionals * Exposure to enterprise-level analytics and ...

Data Analyst

Joliet, IL · On-site

$60 - $80/hr

... Medical Leave, protected veteran status, or any other characteristic protected by law. We prohibit Retaliation against individuals who bring forth any complaint, orally or in writing, to the employer ...

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Medical Device Data Analyst information

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$17

$38

$56

How much do medical device data analyst jobs pay per hour?

As of Sep 8, 2026, the average hourly pay for medical device data analyst in Chicago, IL is $38.46, according to ZipRecruiter salary data. Most workers in this role earn between $25.00 and $39.62 per hour, depending on experience, location, and employer.

What does a medical device data analyst do?

A Medical Device Data Analyst is responsible for collecting, processing, and interpreting data generated from medical devices to support healthcare outcomes, regulatory compliance, and product development. They analyze large datasets to identify trends, ensure data integrity, and provide actionable insights to engineers, clinicians, or regulatory teams. Their work helps improve patient safety, device performance, and supports decision-making processes in medical device companies or healthcare organizations.

How does a medical device data analyst typically collaborate with cross-functional teams in healthcare organizations?

Medical Device Data Analysts frequently work with engineering, clinical, and regulatory teams to interpret and communicate data from medical devices. They analyze device performance and patient outcomes, providing actionable insights that inform product improvements and compliance documentation. Collaboration often includes participating in interdisciplinary meetings, presenting findings, and supporting quality assurance projects. This teamwork ensures the safe and effective use of devices, making strong communication and problem-solving skills essential for success in the role.

What are the key skills and qualifications needed to thrive as a medical device data analyst, and why are they important?

To thrive as a Medical Device Data Analyst, you need strong analytical skills, proficiency in statistics, and a background in life sciences, engineering, or a related field. Expertise in data analysis tools like Python, R, SQL, and familiarity with medical device regulations and systems such as FDA compliance software are typically required. Attention to detail, problem-solving ability, and effective communication are essential soft skills for translating complex data into actionable insights. These competencies are crucial for ensuring data integrity, regulatory compliance, and meaningful contributions to medical device development and patient safety.

What is the difference between Medical Device Data Analyst vs Medical Device Quality Specialist?

AspectMedical Device Data AnalystMedical Device Quality Specialist
Required CredentialsBachelor's in data analysis, healthcare, or related field; certifications like CAP or Six Sigma beneficialBachelor's in engineering, quality assurance, or related; certifications like CQE or ISO auditor often required
Work EnvironmentData analysis teams, R&D, or clinical settings within medical device companiesQuality assurance departments, manufacturing plants, or regulatory compliance teams
Employer & Industry UsageUsed across medical device firms focusing on data management and analysisUsed in quality control, regulatory compliance, and manufacturing sectors

The Medical Device Data Analyst primarily focuses on analyzing data related to medical devices to improve performance and compliance, while the Medical Device Quality Specialist concentrates on ensuring products meet quality standards and regulatory requirements. Both roles are essential in the medical device industry but serve different functions within the product lifecycle.

Are healthcare data analysts in demand?

Healthcare data analysts, including medical device data analysts, are in high demand due to the increasing use of electronic health records and data-driven decision-making in healthcare. They are valued for their skills in data management, analysis tools like SQL and Python, and understanding of medical device data to improve patient outcomes and operational efficiency.

What is a medical device data analyst?

A medical device data analyst is a professional who collects, interprets, and manages data generated by medical devices to ensure device performance, safety, and compliance. They often use data analysis tools and have knowledge of healthcare regulations, working closely with clinical teams to improve device functionality and patient outcomes.

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

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

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

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

Infographic showing various Medical Device Data Analyst job openings in Chicago, IL as of August 2026, with employment types broken down into 68% Full Time, 6% Temporary, and 26% Contract. Highlights an 88% In-person, 6% Hybrid, and 6% Remote job distribution, with an average salary of $79,995 per year, or $38.5 per hour.

DDT Medical Device Investigation Analyst

Takeda Pharmaceuticals

Deerfield, IL • On-site

$89K - $141K/yr

Other

Posted 5 days ago


Takeda Pharmaceuticals rating

7.3

Company rating: 7.3 out of 10

Based on 71 frontline employees who took The Breakroom Quiz

70th of 86 rated pharmaceutical


Job description

DD&T US Medical Device Investigation Analyst

The DD&T US Medical Device Investigation Analyst, reporting to the Plasma-Derived Therapies (PDT) DD&T Operations Lead, is responsible for leading, coordinating, and documenting investigations related to Takeda-developed and owned software and connected medical devices used within U.S. PDT and BioLife operations. This role ensures that device-related complaints, incidents, and quality events are investigated in a timely, compliant, and inspection-ready manner in accordance with FDA Quality System Regulations and Medical Device Reporting (MDR) requirements.

Working closely with DD&T, Quality, Medical Affairs, and Operations, the analyst identifies root causes, assesses potential patient and donor risk, and ensures appropriate linkage to MDRs, deviations, CAPAs, and continuous improvement initiatives. The role plays a critical part in maintaining product quality, regulatory compliance, and operational excellence across the PDT and BioLife network.

Minimum Requirements/Qualifications:

  • Bachelor's degree in computer science, Life Sciences, Quality, or related technical discipline.
  • 2–5 years of experience in medical device investigations, quality assurance, complaint handling, or regulated IT/healthcare environments.
  • Working knowledge of medical device quality system requirements (FDA QSR, ISO 13485 concepts).
  • Experience performing root cause analysis and documenting regulated investigations.
  • Strong written documentation and cross-functional communication skills.
  • Basic knowledge of SQL and at least one programming language.
  • Investigation ownership and critical thinking
  • Risk-based decision making
  • High-quality technical documentation
  • Cross-functional collaboration in regulated environments
  • Regulatory and compliance mindset

Preferred:

  • Experience with software as a medical device (SaMD) or digital health platforms.
  • Familiarity with FDA MDR (21 CFR Part 803) and post-market surveillance support activities.
  • Experience working in plasma collection, biotech, or highly regulated operational environments.
  • Prior support of FDA inspections or quality audits.
  • Experience with Power BI (including building reports and dashboards).

Takeda Compensation and Benefits Summary

We understand compensation is an important factor as you consider the next step in your career. We are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices.

For Location: Bannockburn, IL

U.S. Base Salary Range: $89,900.00 - $141,240.00

The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job. The actual base salary offered will be in accordance with state or local minimum wage requirements for the job location.

For information about our benefits, please click here.

EEO Statement

Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law.

Locations

Bannockburn, IL Cambridge, MA, Exton, PA

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time

Job Exempt

Yes


What Takeda Pharmaceuticals employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom


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About Takeda Ventures

Sourced by ZipRecruiter

Industry

Investment clubs and venture capital companies, pharmaceutical product wholesalers and pharmaceutical and medicine manufacturing

Company size

1 - 10 Employees

Headquarters location

San Diego, CA, US

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