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Regulatory Affairs Jobs (NOW HIRING)

6029-MEDICAL DEVICE BUSINESS SERVICES, INC. Legal Entity

$120 - $180/hr

Represents Regulatory Affairs on cross‑functional project teams. * Partners with other functions to define and obtain data to assist with regulatory submissions. * May work with International ...

Just Energy

Manager Regulatory Affairs

Austin, TX · Remote

Regulatory Affairs Manager - Mass Markets South Location: Remote (Austin, Houston, Dallas, TX areas) Manager Title: Director of Regulatory Affairs, Mass Markets South (Texas, California, Canada ...

ACLD

Regulatory Affairs Analyst

Bethpage, NY · On-site

$66K/yr

Regulatory Affairs Analyst When a group of families came together in 1957 to find services for their children with developmental disabilities, ACLD was born. Today, we are a leading not-for-profit ...

Oterra

Regulatory Affairs Manager

Sturtevant, WI

The Regulatory Affairs Manager is responsible for leading regulatory compliance activities for Oterra's portfolio of natural colors across the United States and Canada. This role provides strategic ...

Legend Biotech US

Director, Regulatory Affairs

Somerset, NJ · Hybrid

$158K - $209K/yr

Legend Biotech is seeking a Director, Regulatory Affairs as part of the Regulatory Affairs team based in Somerset, NJ. Role Overview The Director of Regulatory Affairs is responsible for ...

Actalent

Regulatory Affairs Specialist

Olathe, KS

Regulatory Affairs Specialist / QA-RA Lead This role leads key Quality Assurance and Regulatory Affairs activities to maintain and continually improve the Quality Management System (QMS) for a ...

Oterra

Regulatory Affairs Manager

Mount Pleasant, WI · On-site

The Regulatory Affairs Manager is responsible for leading regulatory compliance activities for Oterra's portfolio of natural colors across the United States and Canada. This role provides strategic ...

Oterra

Regulatory Affairs Manager

Mount Pleasant, WI · On-site

The Regulatory Affairs Manager is responsible for leading regulatory compliance activities for Oterra's portfolio of natural colors across the United States and Canada. This role provides strategic ...

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Regulatory Affairs information

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How much do regulatory affairs jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for regulatory affairs in the United States is $39.57, according to ZipRecruiter salary data. Most workers in this role earn between $31.73 and $46.88 per hour, depending on experience, location, and employer.

What degree do you need for regulatory affairs?

Regulatory affairs professionals typically need at least a bachelor's degree in life sciences, pharmacy, chemistry, or a related field. Advanced roles may require a master's degree or higher, along with knowledge of regulations, good communication skills, and familiarity with regulatory submission processes.

What is regulatory affairs?

Regulatory affairs employees focus on meeting local, national, and international requirements for products. These jobs are particularly common in food, cosmetics, and companies that produce medicine or medical devices. With a position in regulatory affairs, you may be asked to ensure a medicine meets all safety regulations, prepare documents for submission to regulators, monitor translators to ensure the accurate translation of materials as needed, and ensure that records and reports are submitted in line with inspection standards. Regulatory affairs employees also provide support for currently-marketed products and may work with engineering drawings, technical files, or design history files to note required changes.

What do regulatory affairs jobs do?

Regulatory affairs professionals ensure that companies comply with government regulations and industry standards for product development, approval, and marketing. They prepare and submit documentation to regulatory agencies, monitor changes in regulations, and coordinate with cross-functional teams to ensure products meet safety and efficacy requirements throughout their lifecycle.

What are some typical challenges faced by professionals in regulatory affairs, and how can they be managed?

Regulatory Affairs professionals often navigate complex and ever-changing regulations across different regions, which can be challenging when managing multiple submissions or product lines. Staying up-to-date with regulatory updates and effectively communicating requirements to cross-functional teams is essential. Building strong relationships with regulatory agencies and leveraging robust internal processes can help streamline submissions and respond quickly to compliance issues. Proactive planning and regular professional development are key strategies for managing these challenges successfully.

How much do regulatory affairs jobs pay in the US?

Regulatory affairs professionals in the US typically earn a median annual salary of around $100,000, with entry-level positions starting at approximately $70,000 and experienced roles reaching over $130,000. Salaries vary based on experience, industry, location, and certifications such as RAC (Regulatory Affairs Certification).

What is the difference between Regulatory Affairs vs Quality Assurance?

AspectRegulatory AffairsQuality Assurance
Primary FocusEnsuring compliance with regulations and submitting documentation to authoritiesMaintaining product quality and implementing quality systems
Required CredentialsDegree in life sciences, regulatory certifications often preferredDegree in sciences or engineering, quality management certifications
Work EnvironmentRegulatory agencies, corporate compliance teamsManufacturing plants, quality departments
Industry UsagePharmaceuticals, biotech, medical devicesPharmaceuticals, manufacturing, medical devices

While Regulatory Affairs focuses on navigating regulatory requirements and submissions, Quality Assurance emphasizes maintaining product quality standards. Both roles are essential in ensuring products meet industry and legal standards, often collaborating closely within regulated industries.

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What are the most commonly searched types of Regulatory Affairs jobs?

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What states have the most Regulatory Affairs jobs?

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Regulatory Affairs jobs near you
Infographic showing various Regulatory Affairs job openings in the United States as of August 2026, with employment types broken down into 90% Full Time, and 10% Contract. Highlights an 100% In-person job distribution, with an average salary of $82,307 per year, or $39.6 per hour.

Regulatory Affairs Specialist

Stark Pharma Solutions Inc

Franklin Lakes, NJ • On-site

Contractor

Re-posted 5 days ago

Job description

Job Title: Regulatory Affairs Specialist

Locations: New Jersey, Pennsylvania, Massachusetts, Connecticut, Rhode Island, Salt Lake City (UT), California

Duration: Long Term contract

Job Summary

We are seeking experienced Regulatory Affairs professionals to support regulatory strategy, submissions, and compliance activities across pharmaceutical, biotechnology, and medical device programs. This role will work closely with cross-functional teams to ensure products meet global regulatory requirements throughout development, approval, and commercialization.

The ideal candidate will have strong experience with FDA regulations, regulatory submissions, and lifecycle management activities in regulated environments.

Key Responsibilities

  • Prepare, review, and support regulatory submissions including INDs, NDAs, BLAs, 510(k)s, PMAs, amendments, supplements, and annual reports
  • Develop and execute regulatory strategies to support product development and commercialization
  • Ensure compliance with FDA, EMA, ICH, and global regulatory requirements
  • Collaborate with Quality, Clinical, R&D, Manufacturing, and CMC teams on regulatory activities
  • Support change control assessments, labeling updates, and product lifecycle management
  • Review technical documentation, SOPs, and regulatory filings for accuracy and compliance
  • Support regulatory inspections, audits, and agency interactions
  • Monitor evolving regulatory requirements and communicate impact to internal stakeholders

Required Qualifications

  • Bachelor’s degree in Life Sciences, Pharmacy, Regulatory Affairs, Engineering, or related field
  • 3–10+ years of experience in Regulatory Affairs within pharma, biotech, or medical devices
  • Strong knowledge of FDA regulations and global regulatory frameworks
  • Experience supporting regulatory submissions and compliance activities
  • Excellent communication, technical writing, and project management skills
  • Ability to work cross-functionally in fast-paced environments