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Fda Job Jobs (NOW HIRING)

Join us as an FDA Validation Engineer. Location type: This is an onsite position based in Nashville, TN. What We Offer: * Competitive wages, medical benefits starting your first day, and paid ...

Accompany an FDA-commissioned inspector to designated retail locations to assess compliance with tobacco sales regulations. * Attempt to purchase tobacco products while strictly adhering to FDA ...

Accompany an FDA-commissioned inspector to designated retail locations to assess compliance with tobacco sales regulations. * Attempt to purchase tobacco products while strictly adhering to FDA ...

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Fda Job information

What is the difference between Fda Job vs Food Scientist?

AspectFda JobFood Scientist
Required CredentialsBachelor's degree in life sciences, regulatory affairs, or related field; sometimes advanced degreesBachelor's or master's in food science, microbiology, or chemistry
Work EnvironmentRegulatory agencies, laboratories, inspection sitesFood manufacturing facilities, laboratories, research settings
Industry UsageGovernment regulatory body overseeing food safetyPrivate sector food companies, research institutions
Common Search/ComparisonFda Job vs Food ScientistFood Scientist roles and responsibilities

Fda Jobs primarily focus on regulatory compliance, inspections, and policy enforcement within government agencies. Food Scientists, on the other hand, work in research and development, product testing, and improving food safety in private or academic sectors. While both roles involve food safety, Fda Jobs are centered on regulation and oversight, whereas Food Scientists focus on innovation and product quality.

More about Fda Job jobs
What cities are hiring for Fda Job jobs? Cities with the most Fda Job job openings:
What states have the most Fda Job jobs? States with the most job openings for Fda Job jobs include:

Regulatory Affairs Specialist (FDA, DEA )

Barupon LLC

Irvine, CA โ€ข On-site

$60K - $76K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 17 hours ago


Job description

Job Summary
The Regulatory Affairs Specialist (FDA, DEA) will ensure BaRupOn's pharmacy, manufacturing, and healthcare operations meet all applicable regulatory requirements. This position is responsible for preparing submissions, maintaining licenses, coordinating audits, and staying ahead of evolving federal and state regulations related to pharmaceuticals, medical devices, and controlled substances.
Key Responsibilities
  • Prepare and manage FDA submissions (e.g., drug listings, establishment registrations, 503A/503B updates)
  • Oversee and renew DEA registrations, inventory records, and security documentation
  • Maintain state pharmacy, medical device, and wholesale distribution licenses
  • Track regulatory changes affecting compounding, controlled substances, and labeling requirements
  • Support internal audits, site inspections, and responses to 483s or warning letters
  • Coordinate with Quality Assurance on SOP compliance, change controls, and deviation reports
  • Serve as point of contact with federal and state regulatory agencies
  • Document and file compliance records and ensure timely reporting
Qualifications
  • Associate degree in Life Sciences, Regulatory Affairs, or related field (Bachelor's preferred)
  • 2-4 years of regulatory or compliance experience in pharmaceuticals, biotech, or medical devices
  • Working knowledge of FDA regulations (21 CFR Parts 210, 211, 820) and DEA requirements
  • Strong writing, documentation, and organizational skills
  • Familiarity with electronic submission systems, labeling requirements, and drug master files
Preferred Skills
  • Experience in sterile or non-sterile compounding (503A or 503B environments)
  • Knowledge of NABP license portals, MedWatch reporting, or REMS programs
  • Regulatory Affairs Certification (RAC) or DEA compliance training (preferred)
  • Experience responding to FDA inspections, audits, or state pharmacy board requests
Benefits
  • Health, dental, and vision insurance
  • 401(k) with employer match
  • Paid time off and holidays
  • Regulatory training and continuing education support
  • Advancement opportunities into QA/RA leadership roles