ZipRecruiter

Log In

1

Regulatory Affairs Manager Jobs in Springfield, IL

Syneos Health

Field Reimbursement Manager

Springfield, IL · On-site

$90 - $130/hr

Understand all applicable reimbursement regulations for Medicaid, Medicare, and Commercial payers ... We translate unique clinical, medical affairs and commercialinsights into outcomes to address ...

Securitybk

Bank Security Act -BSA Analyst

Springfield, IL · On-site

$52 - $68/hr

Record currency transaction reports in accordance with regulations and guidance from FINCEN prior ... Ability to maintain confidentiality in respect to the customer's financial affairs. Education ...

New

All JobsRegulatory Affairs JobsRegulatory Affairs Manager JobsRegulatory Affairs Manager Jobs in Springfield, IL

Regulatory Affairs Manager information

See Springfield, IL salary details

$28

$56

$85

How much do regulatory affairs manager jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for regulatory affairs manager in Springfield, IL is $56.46, according to ZipRecruiter salary data. Most workers in this role earn between $41.68 and $66.01 per hour, depending on experience, location, and employer.

What does a regulatory affairs manager do?

A Regulatory Affairs Manager oversees the process of ensuring that a company’s products comply with all regulations and laws applicable to their industry, such as pharmaceuticals, medical devices, or food. They coordinate the preparation and submission of regulatory documents to government agencies and serve as a liaison between the company and regulatory authorities. Their role includes monitoring changes in regulations, developing strategies for approval, and ensuring ongoing compliance throughout the product lifecycle.

What does a regulatory affairs manager do?

As a regulatory affairs manager, your responsibilities entail ensuring that your employer observes all relevant laws and regulations. You can find employment in various sectors, including pharmaceutical, healthcare, and manufacturing industries. Your duties include compiling all necessary paperwork, evidence, and documentation to report to regulatory authorities. In addition to the management of paperwork and legal requirements, you help companies make operational and strategic decisions based on the regulations they are obligated to follow. You sometimes perform or coordinate audits to ensure compliance, and, in a large company, you oversee a staff of compliance specialists who handle various regulatory affairs tasks.

What are some common challenges faced by regulatory affairs managers when working with cross-functional teams?

Regulatory Affairs Managers often encounter challenges in aligning regulatory requirements with the goals of other departments, such as R&D, marketing, and manufacturing. Navigating differing priorities and timelines can be complex, especially when ensuring compliance without delaying product development. Effective communication and negotiation skills are essential to bridge gaps between teams, clarify regulatory expectations, and facilitate smooth collaboration. By proactively engaging stakeholders and providing regulatory guidance early in projects, Regulatory Affairs Managers can help teams work together more efficiently and avoid costly compliance issues.

What are the key skills and qualifications needed to thrive as a regulatory affairs manager, and why are they important?

To thrive as a Regulatory Affairs Manager, you need a comprehensive understanding of regulatory guidelines, scientific or technical expertise, and typically a degree in life sciences or a related field. Experience with submission management systems, regulatory databases, and knowledge of global regulatory frameworks (such as FDA, EMA, or ICH) are highly valuable. Strong attention to detail, communication skills, and the ability to manage cross-functional teams distinguish top performers in this role. These competencies are crucial for ensuring product compliance, minimizing approval risks, and facilitating smooth market entry.

What is the difference between Regulatory Affairs Manager vs Regulatory Affairs Specialist?

AspectRegulatory Affairs ManagerRegulatory Affairs Specialist
CredentialsBachelor's degree, often advanced certifications (e.g., RAC)Bachelor's degree, entry-level certifications
Work EnvironmentOversees teams, strategic planning, cross-department collaborationExecutes regulatory submissions, document preparation, detailed compliance tasks
Industry UsageUsed in pharmaceutical, biotech, medical device companies for leadership rolesCommonly found in similar industries, focusing on technical regulatory tasks
Search & Comparison IntentUnderstanding managerial responsibilities and scopeFocus on specific regulatory tasks and compliance details

The Regulatory Affairs Manager typically holds a leadership role, overseeing regulatory strategies and teams, while the Regulatory Affairs Specialist handles detailed compliance work and documentation. Both roles require relevant certifications and are essential in regulated industries like pharma and medical devices.

More about Regulatory Affairs Manager jobs

What job categories do people searching Regulatory Affairs Manager jobs in Springfield, IL look for?

The top searched job categories for Regulatory Affairs Manager jobs in Springfield, IL are:

What cities near Springfield, IL are hiring for Regulatory Affairs Manager jobs?

Cities near Springfield, IL with the most Regulatory Affairs Manager job openings:

Regulatory Affairs Manager jobs near you
Infographic showing various Regulatory Affairs Manager job openings in Springfield, IL as of August 2026, with employment types broken down into 85% Full Time, 13% Part Time, and 2% Contract. Highlights an 88% Physical, 2% Hybrid, and 10% Remote job distribution, with an average salary of $117,439 per year, or $56.5 per hour.

Regulatory Affairs Specialist

Stark Pharma Solutions Inc

Springfield, IL • On-site

Contractor

Re-posted 22 days ago

Job description

Hi,

My name is Sravani Dasari, and I am a Talent Acquisition Specialist with
Stark Pharma Solutions, specializing in opportunities across the
Pharmaceutical, Biotechnology, Medical Device, and Life Sciences industries.
Job Title: Regulatory Affairs Specialist
Location: Springfield, IL
Duration: Long Term

Position Overview

We are seeking a detail-oriented and experienced Regulatory Affairs Specialist to support regulatory compliance activities for medical device products. The ideal candidate will be responsible for preparing regulatory submissions, maintaining product registrations, ensuring compliance with FDA and international regulations, and collaborating with cross-functional teams throughout the product lifecycle.

Key Responsibilities

  • Prepare, review, and submit regulatory documents for product registrations, renewals, and amendments.
  • Support FDA submissions including 510(k), Technical Files, and other regulatory filings as required.
  • Ensure compliance with FDA, ISO 13485, MDR, and other applicable medical device regulations.
  • Maintain regulatory documentation and product registration records.
  • Monitor and interpret changes in regulatory requirements and communicate impacts to internal teams.
  • Collaborate with Quality, R&D, Manufacturing, and Clinical teams to support product development and commercialization.
  • Assist with audits, inspections, and responses to regulatory authorities.
  • Support labelling reviews and regulatory assessments for product changes.

Required Qualifications

  • Bachelor's degree in Regulatory Affairs, Life Sciences, Biomedical Engineering, or a related field.
  • 2+ years of experience in Regulatory Affairs within the Medical Device industry.
  • Knowledge of FDA regulations, 21 CFR Part 820, ISO 13485, and global regulatory requirements.
  • Experience preparing and managing regulatory submissions.
  • Strong documentation, analytical, and organizational skills.
  • Excellent written and verbal communication abilities.
  • Proficiency with Microsoft Office and regulatory document management systems.

I am actively connecting with professionals for current and
upcoming opportunities. If you are open to exploring new roles or would like to
stay informed about relevant positions, please send me your updated resume
along with the best number and time to reach you.
You can also follow Stark Pharma Solutions on LinkedIn for the
latest job updates:
https://www.linkedin.com/company/99455976/