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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 Jun 9, 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 are the key skills and qualifications needed to thrive as a Part Time FDA Regulatory professional, and why are they important?

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 states have the most Part Time Fda Regulatory jobs? States with the most job openings for Part Time Fda Regulatory jobs include:
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 May 2026, with employment types broken down into 73% Full Time, 26% Part Time, and 1% Contract. Highlights an 90% Physical, 1% Hybrid, and 9% 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 - $45/hr

Part-time

Posted 21 days ago

Job description

Regulatory Affairs Manager
Santa Ana, CA
Part-time Approximately 20-25 hours per week

About Huisong:
Founded in 1998, Huisong Pharmaceuticals specializes in the R&D and manufacturing of premium-quality natural ingredients for world-leading companies in the pharmaceutical, nutraceutical, food & beverage, and personal care industries. Today, Huisong Pharmaceuticals is a global operation with an extensive and dynamic product portfolio of natural products and ingredients, remaining firm in its values of "Nature, Health, Science", and continues to advance the world of medicine and nutrition for the well-being of humanity.
Official Company Website: https://www.huisongpharm.com/
Job Description:
  • Develop and execute global regulatory strategies for new and existing products (e.g., dietary supplements, herbal extracts, TCM).
  • Lead FDA submissions (e.g., NDIN, GRAS, OTC monographs) and international registrations (e.g., EU Novel Food, Health Canada NHP).
  • Advise senior management on emerging regulations (e.g., FDA’s NDIN updates, Prop 65, FSMA).
  • Ensure compliance with cGMP, 21 CFR 111/117, ISO 9001, and organic certifications (USDA, EU).
  • Manage regulatory audits (FDA, NSF, customer audits) and lead corrective actions.
  • Oversee labeling and claims review per FDA/FTC guidelines (e.g., structure/function claims, TCM disclosures).
  • Collaborate with R&D, Sales, and Supply Chain to align regulatory requirements with business goals.
  • Liaise with global suppliers to ensure raw material compliance (e.g., adulteration testing, heavy metals, pesticide limits).
  • Navigate TCM-specific regulations (e.g., USP Herbal Compendium, WHO guidelines, China NMPA standards).
  • Address challenges in botanical adulteration, safety data, and traditional use claims.

Education and Experience Requirements:
  • Bachelor's degree or equivalent in pharmacy, chemistry, food science, or herbal medicine; RAC certification a plus.
  • 5+ years in regulatory affairs (nutraceuticals, botanicals, or TCM).
  • Deep knowledge of: FDA 21 CFR 111/117, DSHEA, NDIN, GRAS, cGMP, ISO9001, FSVP, and global supplement regulations.
  • PCQI (Preventive Controls Qualified Individual) certification required; HACCP certification or related food safety training is a plus.