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Part Time Rac Regulatory Affairs Certification Jobs

Harley-Davidson

Sr Regulatory Affairs Engineer

Wauwatosa, WI · On-site

$98K - $135K/yr

Harley-Davidson Motor Company Full or Part-Time: Full Time Shift: SHIFT1 At Harley-Davidson, we are ... Responsible for ongoing certification activities and may lead projects within a broader area.

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How much do part time rac regulatory affairs certification jobs pay per hour?

As of Jun 10, 2026, the average hourly pay for part time rac regulatory affairs certification 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 best regulatory affairs certification?

For regulatory affairs professionals, the Regulatory Affairs Certification (RAC) offered by the Regulatory Affairs Professionals Society (RAPS) is widely recognized as the leading credential. It demonstrates expertise in regulatory processes and compliance across industries such as pharmaceuticals, medical devices, and biotechnology. Earning the RAC can enhance job prospects and credibility in the field.

Can regulatory affairs jobs be done remotely?

Regulatory affairs jobs, including those in the RAC certification field, can often be performed remotely, especially for tasks such as document review, compliance monitoring, and communication with regulatory agencies. However, some roles may require onsite presence for inspections, audits, or meetings with manufacturing teams, depending on company policies and regulatory requirements.

How hard is the RAC exam?

The RAC (Regulatory Affairs Certification) exam is considered challenging, requiring a thorough understanding of regulatory principles, laws, and guidelines. It involves multiple-choice questions and typically requires dedicated study and preparation to pass successfully.

How to get into regulatory affairs with no experience?

Entering regulatory affairs with no experience can be achieved by obtaining relevant certifications such as the RAC, gaining knowledge of industry regulations, and developing skills in compliance, documentation, and communication. Internships or entry-level roles can also provide practical exposure and help build a professional network in the field.

What is the difference between Part Time Rac Regulatory Affairs Certification vs Part Time Regulatory Affairs Specialist?

AspectPart Time Rac Regulatory Affairs CertificationPart Time Regulatory Affairs Specialist
CredentialsCertification focused on RAC standardsTypically requires a degree and experience in regulatory affairs
Work EnvironmentTraining programs, certification coursesOffice, pharmaceutical, or healthcare settings
Employer UsageCertifies individual knowledge and compliancePerforms regulatory submissions and compliance tasks

The Part Time Rac Regulatory Affairs Certification is a credential validating knowledge of regulatory standards, often pursued alongside work. The Part Time Regulatory Affairs Specialist is a role involving hands-on regulatory tasks. Certification enhances credibility, while specialists apply that knowledge in their daily responsibilities.

What are the most commonly searched types of Rac Regulatory Affairs Certification jobs? The most popular types of Rac Regulatory Affairs Certification jobs are:
What states have the most Part Time Rac Regulatory Affairs Certification jobs? States with the most job openings for Part Time Rac Regulatory Affairs Certification jobs include:
Part Time Rac Regulatory Affairs Certification jobs near you

Regulatory Affairs Manager

Huisong Pharmaceuticals

Santa Ana, CA

$38 - $45/hr

Part-time

Posted 22 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.