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Fda Jobs in Chicago, IL (NOW HIRING)

Medline

Sr Product Recall Specialist

Mundelein, IL · On-site

$23.25 - $33.75/hr

Independently manage and respond to FDA effectiveness checks, regulatory inquiries, and followup requests related to recall activities. * Serve as the recall liaison between the company and the FDA ...

Medline

Spec Product Recall Sr

Mundelein, IL

$23.25 - $33.75/hr

Independently manage and respond to FDA effectiveness checks, regulatory inquiries, and followup requests related to recall activities. * Serve as the recall liaison between the company and the FDA ...

Medline

Spec Product Recall Sr

Mundelein, IL · On-site

$23.25 - $33.75/hr

Independently manage and respond to FDA effectiveness checks, regulatory inquiries, and follow‑up requests related to recall activities. Serve as the recall liaison between the company and the FDA ...

Medline

Spec Product Recall Sr

Mundelein, IL · On-site

$23.25 - $33.75/hr

Independently manage and respond to FDA effectiveness checks, regulatory inquiries, and followup requests related to recall activities. * Serve as the recall liaison between the company and the FDA ...

Medline

Spec Product Recall Sr

Mundelein, IL · On-site

$23.25 - $33.75/hr

Independently manage and respond to FDA effectiveness checks, regulatory inquiries, and follow-up requests related to recall activities. * Serve as the recall liaison between the company and the FDA ...

Tempus

Senior Quality Engineer

Chicago, IL · On-site

Be involved in the medical device software design controls activities, in accordance with the FDA Quality System Regulation, ISO 13485, GAMP5, Computer System Validation (CSV) standards and FDA ...

Tempus

Senior Quality Engineer

Chicago, IL · On-site +1

Be involved in the medical device software design controls activities, in accordance with the FDA Quality System Regulation, ISO 13485, GAMP5, Computer System Validation (CSV) standards and FDA ...

Xttrium Laboratories Inc

R&D Scientist

Mount Prospect, IL · On-site

$75K/yr

With over 40 years of expertise in manufacturing FDA-registered healthcare solutions, the company is a leader in ensuring safety and quality in a health-conscious world. Xttrium is looking for an R&D ...

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How much do fda jobs pay per hour?

As of Aug 29, 2026, the average hourly pay for fda in Chicago, IL is $40.39, according to ZipRecruiter salary data. Most workers in this role earn between $25.17 and $50.33 per hour, depending on experience, location, and employer.

What does an FDA professional do?

An FDA professional works for the U.S. Food and Drug Administration, a federal agency responsible for protecting public health by ensuring the safety and efficacy of drugs, medical devices, food, cosmetics, and other products. Their roles can include reviewing and approving new drugs and medical devices, conducting inspections, enforcing regulations, and providing guidance to industries. FDA professionals may also work in research, policy development, and public outreach to ensure that products meet regulatory standards and are safe for consumer use.

What are the key skills and qualifications needed to thrive as an FDA Regulatory Affairs Specialist, and why are they important?

To thrive as an FDA Regulatory Affairs Specialist, you need a strong background in life sciences, regulatory guidelines, and compliance, usually supported by a relevant degree such as pharmacy, biology, or chemistry. Familiarity with regulatory submission systems, FDA regulations (such as 21 CFR), and certifications like RAC (Regulatory Affairs Certification) are highly beneficial. Attention to detail, strong analytical thinking, and effective communication skills help professionals navigate complex regulations and collaborate with cross-functional teams. These competencies ensure that products meet legal requirements and safety standards, facilitating successful approvals and market access.

What are some typical challenges faced by professionals working at the FDA, and how can they be managed?

Professionals at the FDA often navigate complex regulatory requirements, tight deadlines, and the need to balance public health priorities with industry innovation. Collaborating across multidisciplinary teams and staying updated on evolving scientific data are essential parts of the role. Adapting to frequent changes in policy and handling high volumes of submissions can be demanding, but leveraging strong communication skills and seeking mentorship within the agency can help manage these challenges effectively.

What is the difference between Fda vs Food Scientist?

AspectFdaFood Scientist
Required CredentialsTypically a degree in health, science, or related field; certifications varyBachelor's or master's in food science, microbiology, or related
Work EnvironmentRegulatory agencies, laboratories, inspection sitesFood manufacturing facilities, laboratories, research settings
Employer & Industry UsageU.S. Food and Drug Administration, government agenciesFood companies, research institutions, government agencies
Common Search & Comparison IntentUnderstanding regulatory roles, compliance, and enforcementFood safety, product development, research

While both Fda professionals and Food Scientists work within the food industry, Fda roles focus on regulation, compliance, and enforcement of food safety laws, often within government agencies. Food Scientists primarily engage in research, product development, and ensuring food quality in manufacturing settings. The two careers overlap in food safety knowledge but differ in their primary responsibilities and work environments.

What qualifications do you need to work for the Food and Drug Administration?

To work for the Food and Drug Administration (FDA), candidates typically need a bachelor's degree in a relevant field such as science, engineering, or public health. For certain positions, advanced degrees or specialized certifications may be required, along with relevant work experience and knowledge of regulatory processes and compliance standards.

What are the most commonly searched types of Fda jobs in Chicago, IL?

The most popular types of Fda jobs in Chicago, IL are:

What are popular job titles related to Fda jobs in Chicago, IL?

For Fda jobs in Chicago, IL, the most frequently searched job titles are:

What job categories do people searching Fda jobs in Chicago, IL look for?

The top searched job categories for Fda jobs in Chicago, IL are:

What cities near Chicago, IL are hiring for Fda jobs?

Cities near Chicago, IL with the most Fda job openings:

Fda jobs near you
Infographic showing various Fda job openings in Chicago, IL as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 15% Part Time, 3% Contract, and 1% Nights. Highlights an 89% Physical, 2% Hybrid, and 9% Remote job distribution, with an average salary of $84,006 per year, or $40.4 per hour.

Remote Healthcare & FDA Regulatory Law Specialist

Chicago, IL • Remote

Turing
IT Services • 51 - 200 employees
Learn more about Turingexternal

$100 - $200/hr

Contractor

This job post has expired today. Applications are no longer accepted.

Job description

About Turing:
Based in San Francisco, California, Turing is the world’s leading research accelerator for frontier AI labs and a trusted partner for global enterprises deploying advanced AI systems. Turing supports customers in two ways: first, by accelerating frontier research with high-quality data, advanced training pipelines, plus top AI researchers who specialize in coding, reasoning, STEM, multilinguality, multimodality, and agents; and second, by applying that expertise to help enterprises transform AI from proof of concept into proprietary intelligence with systems that perform reliably, deliver measurable impact, and drive lasting results on the P&L.

Role Overview:
Turing invites Healthcare and FDA Regulatory Law experts to join projects that fine-tune AI models like ChatGPT. You will apply your expertise in healthcare compliance, FDA drug/device approval, Anti-Kickback Statute analysis, and HIPAA enforcement to evaluate how AI handles healthcare regulatory scenarios. If you enjoy analyzing Stark Law exceptions, False Claims Act liability, and pre-market approval pathways, this is your opportunity. No prior AI experience is required — your background in U.S. healthcare law is exactly what’s needed.

What Does Day-to-Day Look Like:
  • Review and evaluate AI-generated responses to U.S. healthcare law hypotheticals, including HIPAA privacy and security rules, Anti-Kickback Statute safe harbors, Stark Law exceptions, and FDA approval pathways (510(k), PMA, NDA).
  • Apply a structured legal rubric to assess issue spotting, accuracy of healthcare regulations, and proper application of CMS guidance and FDA rules.
  • Identify gaps in AI reasoning around fraud and abuse compliance, clinical trial regulations, telehealth law, and pharmacy benefit management.
  • Provide detailed, high-quality annotations and written feedback to refine AI models.
  • Collaborate with researchers and project managers to align evaluation standards and project goals. 

Requirements:
  • Juris Doctor (J.D.) from an accredited U.S. law school; Bar admission (active/inactive).
  • 3+ years of U.S. legal practice in healthcare law, FDA regulatory affairs, or healthcare compliance.
  • Strong reasoning skills across HIPAA, the Anti-Kickback Statute, Stark Law, False Claims Act, and FDA regulations.
  • Excellent written communication and attention to detail.
  • High ethical standards; interest in AI is a plus.

Perks of Freelancing with Turing:
  • Opportunity to work on cutting-edge AI projects with leading LLM companies.
  • Competitive compensation.
  • Flexible, fully remote work arrangement.
  • Learn how to use AI to advance the legal field.

Offer Details:
  • Commitment: Flexible, 10–30 hrs/week.
  • Duration: ~1 month, with the possibility of extension based on performance and project needs.