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Regulatory Affairs Science Jobs (NOW HIRING)

CICONIX, LLC

Senior Regulatory Affairs Scientist About CICONIX: CICONIX LLC is a Veteran Owned Small Business specializing in business advisory and technical assistance for military health programs. We value ...

Vital Connect Inc

Regulatory Affairs Director

CA · Remote

$150K - $175K/yr

Description Purpose Responsible for regulatory affairs activities such as regulatory submissions ... Scientific knowledge, must be able to digest complex data while keeping the big picture through ...

5TH HQ LLC

Regulatory Affairs

Fort Lauderdale, FL · On-site

$19 - $20/hr

Bachelor's degree in a related field such as biology, chemistry, or pharmaceutical sciences. * Previous experience in a regulatory affairs role within the pharmaceutical industry is preferred.

TeamSoft

$22 - $25/hr

Food Science Admin (Regulatory Affairs) Opening Location: East Hanover, NJ. Onsite M-F. Ongoing contract (minimum 1+ years in duration) Pay rate: $22-25/hr Zing Recruiting, in partnership with an ...

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Regulatory Affairs Science information

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$15

$34

$145

How much do regulatory affairs science jobs pay per hour?

As of Jul 18, 2026, the average hourly pay for regulatory affairs science in the United States is $34.60, according to ZipRecruiter salary data. Most workers in this role earn between $22.36 and $26.20 per hour, depending on experience, location, and employer.

What is the highest paying job in regulatory affairs?

The highest paying roles in regulatory affairs are typically senior executive positions such as Director of Regulatory Affairs or Vice President of Regulatory Affairs, which can offer salaries exceeding $150,000 annually. These roles require extensive experience, leadership skills, and often advanced certifications like RAC (Regulatory Affairs Certification).

What does a regulatory affairs scientist do?

A regulatory affairs scientist ensures that products such as pharmaceuticals, medical devices, or food items comply with government regulations and standards. They prepare and review documentation for regulatory submissions, monitor changes in regulations, and collaborate with development teams to facilitate product approval processes. Strong knowledge of regulatory guidelines and attention to detail are essential in this role.

What are Regulatory Affairs Science professionals?

Regulatory Affairs Science professionals are specialists who ensure that companies comply with all regulations and laws pertaining to their business, particularly in industries such as pharmaceuticals, medical devices, biotechnology, and food. They are responsible for preparing and submitting regulatory documents to government agencies, monitoring changes in regulations, and advising their organizations on compliance strategies. Their work helps ensure that products are safe, effective, and meet all legal requirements before being marketed to the public.

What are the key skills and qualifications needed to thrive as a Regulatory Affairs Science professional, and why are they important?

To thrive as a Regulatory Affairs Science professional, you need a solid background in life sciences, regulatory guidelines, and compliance standards, typically supported by a relevant science degree. Familiarity with regulatory databases, submission management systems, and certifications like RAC (Regulatory Affairs Certification) are highly valuable. Strong attention to detail, effective communication, and problem-solving skills help you navigate complex regulations and collaborate with cross-functional teams. These competencies are crucial to ensure successful product approvals and maintain compliance with evolving global regulations.

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

AspectRegulatory Affairs ScienceRegulatory Affairs Specialist
Required CredentialsBachelor's or higher in life sciences, certifications like RAC often preferredBachelor's degree in life sciences or related field, certifications like RAC beneficial
Work EnvironmentResearch labs, regulatory departments, cross-functional teamsRegulatory departments, client interactions, documentation review
Employer & Industry UsagePharmaceutical, biotech, medical device companiesPharmaceutical, biotech, medical device companies
Common Search & ComparisonYesYes

Regulatory Affairs Science professionals focus on scientific and technical aspects of regulatory submissions, often involved in research and data analysis. Regulatory Affairs Specialists handle documentation, compliance, and communication with regulatory agencies. Both roles are essential in ensuring product approval and compliance within the same industries, but they differ in their core responsibilities and focus areas.

Will AI replace regulatory affairs?

AI is increasingly used to support regulatory affairs professionals by automating data analysis, document review, and compliance tracking. However, regulatory affairs roles require critical thinking, interpretation of regulations, and communication skills that are not easily replaced by AI, making human expertise essential in the field.

What are some common challenges faced in a Regulatory Affairs Science role, and how can professionals prepare for them?

Professionals in Regulatory Affairs Science often face the challenge of keeping up with constantly evolving regulations across multiple regions. Navigating differing international standards, managing tight submission deadlines, and ensuring thorough documentation can be demanding. Building strong cross-functional communication skills and staying current with industry updates are essential strategies for overcoming these challenges. Participating in ongoing training and networking with regulatory professionals also helps in staying informed and prepared.

What can you do with a Regulatory Science degree?

A Regulatory Affairs Science degree prepares individuals for roles in ensuring products meet regulatory standards, such as in pharmaceuticals, medical devices, or food industries. Graduates can work as regulatory specialists, compliance managers, or in quality assurance, often utilizing knowledge of regulations, documentation, and submission processes to facilitate product approval and market access.
More about Regulatory Affairs Science jobs
What cities are hiring for Regulatory Affairs Science jobs? Cities with the most Regulatory Affairs Science job openings:
What states have the most Regulatory Affairs Science jobs? States with the most job openings for Regulatory Affairs Science jobs include:
What job categories do people searching Regulatory Affairs Science jobs look for? The top searched job categories for Regulatory Affairs Science jobs are:
Regulatory Affairs Science jobs near you
Infographic showing various Regulatory Affairs Science job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 76% Full Time, 20% Part Time, 1% Temporary, and 2% Contract. Highlights an 79% Physical, 2% Hybrid, and 19% Remote job distribution, with an average salary of $71,960 per year, or $34.6 per hour.
Senior Regulatory Affairs Scientist

Senior Regulatory Affairs Scientist

Venesco LLC

Falls Church, VA • On-site

Full-time

Posted 11 days ago

Job description

Senior Regulatory Affairs Scientist
Location: Hybrid
Job Type: Full-Time
About the Role
Join a dynamic regulatory team as a Senior Regulatory Affairs Scientist, where you will lead submission strategies and regulatory interactions for innovative medical products.
Key Responsibilities
  • Develop and execute regulatory strategies and submission plans
  • Prepare and submit INDs, NDAs, BLAs, and IDEs
  • Serve as primary liaison with FDA and regulatory agencies
  • Provide regulatory guidance to cross-functional teams
  • Monitor regulatory trends and ensure compliance with evolving requirements
  • Review and approve regulatory documentation

Requirements
Qualifications
  • Advanced degree in regulatory science, biology, or related field
  • 8+ years of regulatory affairs experience
  • Strong knowledge of FDA regulations and ICH guidelines

Preferred
  • RAC certification
  • Experience with electronic submissions (eCTD)

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