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Regulatory Affairs Jobs (NOW HIRING)

Regulatory Affairs

Fort Lauderdale, FL ยท On-site

$19 - $20/hr

We are currently seeking a detail-oriented and motivated Regulatory Affairs Specialist. This role is crucial in ensuring that our products comply with all regulatory requirements. If you are ...

The Regulatory Affairs Specialist will be responsible for regulatory documentation, compliance, requirements, submissions, and overall regulatory affairs activities. Qualifications * Regulatory ...

Manager, Regulatory Affairs Location US-WA-Bothell ID 2026-1797 Position Type Full Time Work Model Hybrid Company Overview Verathon is a global medical device company focused on supporting customers ...

The Manager, Regulatory Affairs leads the Regulatory Affairs function, managing the discipline through Regulatory Affairs Specialists and, as the team scales, subordinate supervisors responsible for ...

We're hiring a Analyst, Regulatory Affairs to join our Regulatory Affairs team. Oscar is the first health insurance company built around a full stack technology platform and a relentless focus on ...

The Manager, Regulatory Affairs leads the Regulatory Affairs function, managing the discipline through Regulatory Affairs Specialists and, as the team scales, subordinate supervisors responsible for ...

Makes a proactive contribution to the overall Regulatory affairs department growth. * Provides general regulatory consultation during absence of other associates. * Participates in project ...

Analyst, Regulatory Affairs

Atlanta, GA ยท Remote

$28.30 - $37.15/hr

We're hiring a Analyst, Regulatory Affairs to join our Regulatory Affairs team. Oscar is the first health insurance company built around a full stack technology platform and a relentless focus on ...

We're hiring a Analyst, Regulatory Affairs to join our Regulatory Affairs team. Oscar is the first health insurance company built around a full stack technology platform and a relentless focus on ...

Analyst, Regulatory Affairs

Dallas, TX ยท Remote

$28.30 - $37.15/hr

We're hiring a Analyst, Regulatory Affairs to join our Regulatory Affairs team. Oscar is the first health insurance company built around a full stack technology platform and a relentless focus on ...

As a Regulatory Affairs Specialist, you will be part of the Regulatory Affairs Department supporting global post-market compliance activities. The ideal candidate will have attention to detail ...

Regulatory Affairs Manager - Mass Markets South Location: Remote (Austin, TX) Manager Title: Director of Regulatory Affairs, Mass Markets South (Texas, California, Canada) Position Overview The ...

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Regulatory Affairs information

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$18

$39

$62

How much do regulatory affairs jobs pay per hour?

As of Jul 28, 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 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 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.

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

To thrive as a Regulatory Affairs professional, you need a strong understanding of regulatory guidelines, compliance standards, and scientific or technical documentation, often supported by a degree in life sciences, pharmacy, or a related field. Familiarity with regulatory submission systems, document management tools, and certifications like RAC (Regulatory Affairs Certification) are commonly required. Excellent attention to detail, project management, and effective communication skills help professionals navigate complex regulations and collaborate with cross-functional teams. These competencies ensure timely product approvals, minimize compliance risks, and facilitate successful market access for products.

What are Regulatory Affairs?

Regulatory Affairs is a field focused on ensuring that companies comply with all of the regulations and laws pertaining to their business, particularly in industries such as pharmaceuticals, biotechnology, medical devices, and food. Professionals in Regulatory Affairs help guide products through the approval process by preparing and submitting required documentation to regulatory agencies like the FDA or EMA. They also monitor changes in regulations, advise on compliance strategies, and help organizations maintain market access for their products. This role is crucial for minimizing legal risks and ensuring the safety and efficacy of products.

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.

What cities are hiring for Regulatory Affairs jobs? Cities with the most Regulatory Affairs job openings:
What are the most commonly searched types of Regulatory Affairs jobs? The most popular types of Regulatory Affairs jobs are:
What states have the most Regulatory Affairs jobs? States with the most job openings for Regulatory Affairs jobs include:
Infographic showing various Regulatory Affairs job openings in the United States as of July 2026, with employment types broken down into 77% Full Time, 20% Part Time, 1% Temporary, and 2% Contract. Highlights an 80% Physical, 3% Hybrid, and 17% Remote job distribution, with an average salary of $82,307 per year, or $39.6 per hour.
Regulatory Affairs

Regulatory Affairs

5TH HQ LLC

Fort Lauderdale, FL โ€ข On-site

$19 - $20/hr

Full-time

Posted 5 days ago


Job description

We are currently seeking a detail-oriented and motivated Regulatory Affairs Specialist. This role is crucial in ensuring that our products comply with all regulatory requirements. If you are passionate about regulatory affairs and looking for an opportunity to grow within a dynamic company, we encourage you to apply.

Responsibilities:

  • Prepare, review, and submit regulatory documents to ensure compliance with FDA and other regulatory authorities.
  • Maintain up-to-date knowledge of regulations, guidelines, and standards relevant to the pharmaceutical industry.
  • Assist in the preparation of regulatory submissions including New Drug Applications (NDAs), Investigational New Drug Applications (INDs), and amendments.
  • Coordinate with cross-functional teams to gather necessary information for regulatory submissions.
  • Ensure timely and accurate communication with regulatory authorities.
  • Monitor and track the progress of submissions and respond to any inquiries from regulatory bodies.
  • Assist in the development and implementation of regulatory strategies to support product approvals and lifecycle management.
  • Maintain accurate and organized regulatory files and records.

Requirements:

  • Bachelorโ€™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.
  • Strong understanding of FDA regulations and guidelines.
  • Excellent organizational and time management skills.
  • Strong attention to detail and ability to handle multiple projects simultaneously.
  • Effective communication skills, both written and verbal.
  • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
  • Ability to work independently and as part of a team.

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About 5th HQ

Sourced by ZipRecruiter

We are a boutique Staffing & Recruiting agency that provides a full range of employment solutions that include full-time, temporary, and part-time employment in a wide range of positions, including Professional, Light Industrial, and Office Services.

Industry

Recruiting and staffing services

Headquarters location

Plantation, FL, US