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Part Time Fda Regulatory Jobs (NOW HIRING)

Aegis Ventures

Clinical Affairs Manager (Part-Time)

$135 - $175/hr

About the Job As the Clinical Affairs Manager (Part-Time) , you will lead clinical affairs and ... Support FDA regulatory pathway including Q-sub preparation and clinical trial protocols * Oversee ...

Bizzell Group

Central North Carolina (Triangle Region) Job Type: Part-Time, Temporary Headquarters: New ... This position plays a critical role in supporting federal and state regulatory enforcement by ...

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Part Time Fda Regulatory information

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How much do part time fda regulatory jobs pay per hour?

As of Aug 4, 2026, the average hourly pay for part time fda regulatory 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 difference between Part Time Fda Regulatory vs Part Time Fda Compliance Specialist?

AspectPart Time Fda RegulatoryPart Time Fda Compliance Specialist
Required CredentialsRegulatory Affairs Certification, Bachelor's in Life SciencesRegulatory Affairs Certification, Bachelor's in Life Sciences
Work EnvironmentRegulatory departments, offices, labsQuality assurance, regulatory departments, offices
Employer & Industry UsageMedical device, pharmaceutical companiesMedical device, pharmaceutical companies
Common Search & ComparisonYesYes

Part Time Fda Regulatory and Part Time Fda Compliance Specialist roles often overlap in credentials, work environment, and industry. Both require similar certifications and are found in regulated industries like pharmaceuticals and medical devices. The main difference lies in focus: Fda Regulatory roles emphasize navigating FDA regulations and submissions, while Compliance Specialists focus on ensuring ongoing adherence to those regulations within organizations.

What are the most common challenges faced by part time FDA Regulatory professionals, and how can they be managed?

Part-time FDA Regulatory professionals often face the challenge of staying up-to-date with rapidly changing regulations while managing limited working hours. Balancing multiple projects, meeting tight submission deadlines, and maintaining clear communication with cross-functional teams can also be demanding. To overcome these challenges, it's important to set clear priorities, use efficient workflow tools, and stay proactive about regulatory updates. Open communication with supervisors and colleagues helps ensure alignment and smooth information flow, even with a part-time schedule.

What does a part time FDA Regulatory professional do?

A Part Time FDA Regulatory professional helps organizations comply with regulations set by the U.S. Food and Drug Administration (FDA). Their responsibilities often include reviewing documentation, preparing submissions, and advising on compliance for products such as drugs, medical devices, food, or cosmetics. Working part-time, they may focus on specific projects or provide ongoing support to regulatory teams. Their expertise ensures that products meet all necessary legal and safety standards before and after they reach the market.

What skills and qualifications are needed to thrive as a part time FDA Regulatory professional?

To thrive as a Part Time FDA Regulatory professional, you need strong knowledge of FDA regulations, compliance standards, and documentation practices, often supported by a degree in life sciences or a related field. Familiarity with regulatory submission systems, such as eCTD, and certifications like RAC (Regulatory Affairs Certification) are highly valued. Attention to detail, strong organizational skills, and effective communication are crucial soft skills for managing complex regulatory processes and collaborating with cross-functional teams. These competencies ensure that products meet legal requirements and reach the market efficiently while maintaining compliance and minimizing risk.
More about Part Time Fda Regulatory jobs
What cities are hiring for Part Time Fda Regulatory jobs? Cities with the most Part Time Fda Regulatory job openings:
What are the most commonly searched types of Fda Regulatory jobs? The most popular types of Fda Regulatory jobs are:
What job categories do people searching Part Time Fda Regulatory jobs look for? The top searched job categories for Part Time Fda Regulatory jobs are:
Part Time Fda Regulatory jobs near you
Infographic showing various Part Time Fda Regulatory job openings in the United States as of July 2026, with employment types broken down into 100% Part Time. Highlights an 96% In-person, and 4% Remote job distribution, with an average salary of $71,960 per year, or $34.6 per hour.

Regulatory Affairs Manager

Huisong Pharmaceuticals

Santa Ana, CA • On-site

$38 - $48/hr

Part-time

Re-posted 17 days ago

Job description

Regulatory Affairs Manager
Company: Huisong Inc.
Location: Santa Ana, California, Orange County
Schedule: Part-time, approximately 10 hours per week
Work Arrangement: On-site
About Huisong Inc.
Huisong Inc., located in Santa Ana, California, is the U.S. office of Huisong Pharmaceuticals. Founded in 1998, Huisong Pharmaceuticals specializes in the research, development, and manufacturing of premium-quality natural ingredients for leading companies in the pharmaceutical, nutraceutical, food and beverage, and personal care industries. Today, Huisong Pharmaceuticals operates globally and offers an extensive portfolio of natural products and ingredients. Guided by its core values of Nature, Health, and Science, Huisong continues to advance medicine and nutrition in support of health and well-being worldwide.
Official Company Website: https://www.huisongpharm.com/
Position Overview
Huisong Inc. is seeking an experienced Regulatory Affairs Manager to support regulatory strategy and compliance for dietary supplements, botanical ingredients, herbal extracts, and Traditional Chinese Medicine products.
The Regulatory Affairs Manager will support the U.S. business while collaborating with Huisong’s corporate office, global teams, suppliers, and business partners.
Key Responsibilities:
  • Develop and implement regulatory strategies for new and existing products, including dietary supplements, herbal extracts, botanical ingredients, and Traditional Chinese Medicine products.
  • Lead or support FDA submissions and regulatory pathways, including New Dietary Ingredient Notifications, GRAS determinations, and applicable OTC monograph requirements.
  • Support international product registrations, including EU Novel Food applications and Health Canada Natural Health Product registrations.
  • Advise senior management on new and emerging regulations, including FDA updates, California Proposition 65, FSMA, and international regulatory developments.
  • Ensure compliance with applicable current Good Manufacturing Practices, including 21 CFR Parts 111 and 117, ISO 9001 standards, and USDA and EU organic certification requirements.
  • Manage FDA, NSF, customer, and third-party regulatory audits and oversee corrective and preventive actions.
  • Review product labels, marketing materials, and product claims for compliance with FDA and FTC requirements, including structure/function claims and Traditional Chinese Medicine disclosures.
  • Collaborate with Research and Development, Sales, Quality, and Supply Chain teams to align regulatory requirements with business goals.
  • Work with global suppliers to ensure raw material compliance, including ingredient identity, adulteration testing, heavy metal limits, pesticide limits, and supporting documentation.
  • Navigate regulations and standards specific to botanicals and Traditional Chinese Medicine, including the USP Herbal Medicines Compendium, World Health Organization guidance, and China NMPA standards.
  • Address regulatory matters involving botanical adulteration, safety data, ingredient identity, and traditional-use claims.

Education and Experience Requirements:
  • Bachelor’s degree or equivalent education in pharmacy, chemistry, food science, herbal medicine, regulatory affairs, or a related scientific field.
  • At least five years of regulatory affairs experience within the nutraceutical, dietary supplement, botanical, herbal medicine, or Traditional Chinese Medicine industries.
  • Strong working knowledge of:
    • FDA 21 CFR Parts 111 and 117
    • Dietary Supplement Health and Education Act
    • New Dietary Ingredient Notifications
    • GRAS requirements
    • Current Good Manufacturing Practices
    • ISO 9001
    • Foreign Supplier Verification Programs
    • U.S. and international dietary supplement regulations
  • Preventive Controls Qualified Individual certification is required.
  • HACCP certification or related food-safety training is preferred.
  • Regulatory Affairs Certification is a plus.

Additional Qualifications:
  • Experience managing FDA, customer, or third-party certification audits.
  • Experience working with international suppliers and corporate teams.
  • Strong analytical, communication, organizational, and documentation skills.
  • Ability to interpret complex regulatory requirements and provide practical guidance to leadership and cross-functional teams.
  • Ability to work independently and manage priorities within a part-time schedule.