Regulatory Affairs Analyst Jobs in Illinois
Regulatory affairs analyst jobs in Illinois are concentrated in life sciences, pharmaceuticals, and medical devices, with the state ranking among the most active markets in the country for this specialty. The heaviest hiring is in and around Chicago, Deerfield, and North Chicago, where companies like Abbott, Baxter International, and Takeda have long-standing operations. The most in-demand sub-areas are FDA regulatory submissions, quality management systems, and combination product compliance. Scan the live roles below and apply to whichever ones fit.
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Showing 5 of 39+ Regulatory Affairs Analyst jobs
Expected pay for this position is $36.04 - $42.40/hour. Actual pay will be determined by experience, skills and internal equity. This is a Salaried position.
POSITION SUMMARY: The Regulatory Affairs Specialist serves as the subject matter expert (SME) for all accreditation, certification, and regulatory programs (e.g., TJC, IDPH, specialty certifications) and is accountable for providing feedback to operating units for continuous survey readiness and sustained compliance. This role leads mock surveys, tracers, and readiness assessments; prepares and submits regulatory violation responses; facilitates recovery and performance improvement efforts; and monitors corrective action plans for completion and effectiveness. In partnership with clinical and operational leaders, the Specialist proactively identifies regulatory risk, develops and communicates an annual risk assessment to prioritize high‑risk monitoring, and serves as a primary liaison during surveys and certifications. The role provides expert regulatory guidance and supports quality, safety, and compliance goals.
Education: Bachelor’s degree in a clinical field
Experience: 2 years of practice in healthcare area of expertise
Other Skills/ Knowledge:
- Excellent interpersonal and communication skills.
- Solid computer skills, including proficiency with Microsoft software.
- Strong analytical and problem-solving skills, with the ability to be detail oriented.
PREFERRED QUALIFICATIONS:
Expected pay for this position is $36.04 - $42.40/hour. Actual pay will be determined by experience, skills and internal equity. This is a Salaried position.
POSITION SUMMARY: The Regulatory Affairs Specialist serves as the subject matter expert (SME) for all accreditation, certification, and regulatory programs (e.g., TJC, IDPH, specialty certifications) and is accountable for providing feedback to operating units for continuous survey readiness and sustained compliance. This role leads mock surveys, tracers, and readiness assessments; prepares and submits regulatory violation responses; facilitates recovery and performance improvement efforts; and monitors corrective action plans for completion and effectiveness. In partnership with clinical and operational leaders, the Specialist proactively identifies regulatory risk, develops and communicates an annual risk assessment to prioritize high‑risk monitoring, and serves as a primary liaison during surveys and certifications. The role provides expert regulatory guidance and supports quality, safety, and compliance goals.
Education: Bachelor’s degree in a clinical field
Experience: 2 years of practice in healthcare area of expertise
Other Skills/ Knowledge:
- Excellent interpersonal and communication skills.
- Solid computer skills, including proficiency with Microsoft software.
- Strong analytical and problem-solving skills, with the ability to be detail oriented.
PREFERRED QUALIFICATIONS:
See All 39 Regulatory Affairs Analyst Jobs in Illinois
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Find JobsRegulatory Affairs Analyst Jobs by City in Illinois
Where Illinois roles are concentrated, by current openings.
Regulatory Affairs Analyst Job Market in Illinois
A snapshot from current Illinois openings, updated as new roles post.
Who's Hiring
- Katalyst Healthcares & Life Sciences10
- AbbVie6
- Mars3
- OSF HealthCare3
- Covista2
Top Industries Hiring
- Consulting & Professional Services
- Food & Beverage
- Agriculture & Farming
What Illinois Employers Look For
The qualifications that appear most often in regulatory affairs analyst jobs across Illinois.
- Bachelor's degree in life sciences, chemistry, engineering, or a closely related field
- Experience with FDA submissions including 510(k), PMA, NDA, or BLA filings
- Familiarity with CFR Title 21 and ICH guidelines for pharmaceutical or device products
- Proficiency with regulatory information management systems such as Veeva Vault
- Strong technical writing skills for preparing regulatory dossiers and responses
- RAC credential from the Regulatory Affairs Professionals Society preferred by many Illinois employers
Regulatory Affairs Analyst Jobs in Illinois: Frequently Asked Questions
How do you become a regulatory affairs analyst in Illinois?
Most Illinois employers require at minimum a bachelor's degree in a life science, pharmacy, engineering, or a related technical field, with pharmaceutical and medical device companies often preferring candidates who also hold the Regulatory Affairs Certification from the Regulatory Affairs Professionals Society. Illinois does not issue a state-specific license for this role, so the RAC credential and hands-on experience with FDA submissions are the primary differentiators that hiring managers in the Chicago metro and North Shore corridor look for.
Which companies hire regulatory affairs analysts in Illinois?
Employers hiring regulatory affairs analysts in Illinois right now include Katalyst Healthcares & Life Sciences, AbbVie, and Mars, based on current listings on Migrate Mate as of November 2026. Illinois's dense concentration of pharmaceutical headquarters and medical device manufacturers along the North Shore and in the Chicago suburbs makes it one of the country's most consistent sources of regulatory affairs openings.
Which Illinois cities have the most regulatory affairs analyst jobs?
The cities with the most regulatory affairs analyst openings in Illinois are Chicago, North Chicago, and Mettawa. The distribution follows the state's life sciences footprint, with the greater Chicago area anchoring demand through its pharmaceutical and medical device headquarters, while suburban corridors like Deerfield and North Chicago generate significant volume because of the large campuses Abbott and Baxter maintain there.
Are there remote regulatory affairs analyst jobs in Illinois?
Yes, and more than most fields, since regulatory affairs work is largely document-driven and does not require a physical presence on a production floor. About 94% of regulatory affairs analyst openings tied to Illinois are remote or hybrid as of November 2026, reflecting broad employer acceptance of distributed work for this role. Submission writing, labeling review, and regulatory strategy work are the functions most likely to be listed as fully remote.
How can I get hired as a regulatory affairs analyst in Illinois with little or no experience?
The most realistic entry path is a lateral move from a quality assurance, clinical research, or regulatory operations role at a pharmaceutical or medical device company, since Illinois employers like Abbott, Baxter, and Takeda regularly post associate regulatory affairs positions that are explicitly open to candidates with adjacent scientific experience. Pursuing the Regulatory Affairs Professionals Society's RAC exam prep or completing a post-baccalaureate regulatory affairs certificate through a Chicago-area university also signals commitment that hiring managers respond to when a candidate's direct submission experience is limited.
Where can I find and apply to regulatory affairs analyst jobs in Illinois?
You can find and apply to regulatory affairs analyst jobs in Illinois on Migrate Mate, which lists current Illinois openings updated on an ongoing basis. Search the listings, find the roles that match your background and target companies, and apply directly to whichever ones fit your experience level and location preferences.
See All 39 Regulatory Affairs Analyst Jobs in Illinois
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