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Part Time Fda Consulting 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 ... Partner with regulatory consultants on FDA strategy and submissions * Collaborate with algorithm ...

Kamada

Product Consultant

With a diverse portfolio of FDA-approved products, a strong development pipeline, and industry ... This is a part-time, exempt, salaried position and is not eligible for company benefits. Why Work ...

LaserAway

Registered Nurse - Part Time

Pittsburgh, PA

$40/hr

... consultations; designing individualized treatment plans; documenting accurately; and partnering ... And as we continuously add the latest FDA-cleared technologies to our treatment menu, you'll always ...

LaserAway

Registered Nurse - Part Time

Pittsburgh, PA · On-site

$40/hr

... consultations; designing individualized treatment plans; documenting accurately; and partnering ... And as we continuously add the latest FDA-cleared technologies to our treatment menu, you'll always ...

OncoHealth

Medical Director (Part-Time)

... consultations with treating physicians, as needed * Quality improvement activities focused on ... Since 2018, the FDA approved 121 new cancer applications including 49 novel cancer drug entities.

MyMenopauseRx

Physician

Wheaton, IL · On-site +1

... FDA-approved hormone therapy and non-hormonal options, all covered by health insurance. Through ... Join us in revolutionizing women's healthcare! About the Role We are seeking a part-time tech-savvy ...

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Part Time Fda Consulting information

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$33

$53

$60

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

As of Jun 9, 2026, the average hourly pay for part time fda consulting in the United States is $53.84, according to ZipRecruiter salary data. Most workers in this role earn between $53.61 and $58.89 per hour, depending on experience, location, and employer.

What is the difference between Part Time Fda Consulting vs Part Time Fda Regulatory Affairs Specialist?

AspectPart Time Fda ConsultingPart Time Fda Regulatory Affairs Specialist
CredentialsTypically requires knowledge of FDA regulations, industry experience, and possibly certifications like RACRequires similar credentials, including FDA regulatory knowledge and certifications such as RAC or equivalent
Work EnvironmentConsulting firms, freelance projects, or contract roles with multiple clientsIn-house or consulting roles within medical device, pharmaceutical, or biotech companies
Employer & Industry UsageUsed by consulting agencies, freelance professionals, and contract workers in FDA-regulated industriesCommonly employed by pharmaceutical, biotech, and medical device companies, or consulting firms

Both roles require FDA regulatory knowledge and certifications like RAC. However, Part Time Fda Consulting typically involves freelance or contract work across multiple clients, while Part Time Fda Regulatory Affairs Specialists are usually employed directly by companies or consulting firms to handle regulatory submissions and compliance within specific organizations.

More about Part Time Fda Consulting jobs
What are the most commonly searched types of Fda Consulting jobs? The most popular types of Fda Consulting jobs are:
What job categories do people searching Part Time Fda Consulting jobs look for? The top searched job categories for Part Time Fda Consulting jobs are:
Part Time Fda Consulting jobs near you
Infographic showing various Part Time Fda Consulting job openings in the United States as of June 2026, with employment types broken down into 64% Full Time, and 36% Part Time. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $111,985 per year, or $53.8 per hour.
Commissioned Inspector - FDA Tobacco Inspection Program

Commissioned Inspector - FDA Tobacco Inspection Program

Bizzell Group

Charlotte, NC • On-site, Remote

Part-time

Posted 17 days ago

Job description

Location: Statewide, North Carolina
Job Type: Contract, Part-Time
Headquarters: New Carrollton, MD
Overview
Bizzell is a consulting, strategy, investment and technology firm with a mission to improve lives and accelerate positive change. We deliver award-winning services to a diverse portfolio of clients to help build healthy, secure, connected and sustainable communities in our nation and around the world. Bizzell's multi-disciplinary team works in health solutions, workforce innovation, managed services, and global programs. Specifically, they offer expertise in program management, research and evaluation, communication and outreach, training and technical assistance, policy analysis, and development.
Key Responsibilities
Compliance Inspections & Enforcement
  • Conduct Undercover Buy (UB) and Advertising & Labeling (A&L) inspections at licensed tobacco retail outlets.
  • Ensure compliance with FDA and North Carolina guidelines related to tobacco sales and marketing.
  • Properly document findings and maintain compliance with chain of custody protocols for evidence storage.
  • Coordinate with state and federal program officials to support compliance enforcement actions.
  • Provide testimony and declarations for enforcement or judicial actions when required.

Data Collection & Reporting
  • Accurately enter inspection results into the FDA Tobacco Inspection Management System (TIMS).
  • Prepare and submit detailed reports on findings in alignment with FDA program requirements.
  • Participate in routine quality assurance reviews to ensure inspection accuracy and procedural adherence.

Training & Professional Development
  • Complete annual training and certification to maintain FDA Commissioned Inspector status.
  • Attend regular program meetings and refresher training sessions to stay updated on federal and state regulations.

Why Join Us?
  • Make an impact by enforcing tobacco control laws that protect public health.
  • Gain valuable experience in regulatory enforcement and federal compliance programs.
  • Work as part of a highly trained team dedicated to upholding public health and safety standards.

Interested candidates should submit their resume and cover letter, detailing relevant experience and qualifications.
Requirements
Education & Experience
  • Law enforcement or regulatory compliance experience is strongly preferred.
  • Strong attention to detail and the ability to follow strict compliance protocols.

Additional Requirements
  • Ability to work flexible hours and travel statewide as needed.
  • Must be able to pass a FDA clearance.
  • Must have a valid driver's license and reliable transportation.

Technical & Administrative Skills
  • Ability to document findings accurately and submit reports in a timely manner.
  • Strong communication and observational skills
  • Familiarity with federal and state tobacco control laws is a plus.

Apply