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From Home Fda Inspector Jobs (NOW HIRING)

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Counsel clients regarding FDA regulations, guidance, inspections, investigations, warning letters ... J.D. from an accredited law school. * Licensed and in good standing in at least one U.S ...

Prepare clients for inspections, provide inspection support (remote and on-site) * Provide ... Interpersonal skills necessary in order to communicate and follow instructions effectively from a ...

Home Inspector

Raleigh, NC · On-site

$35K - $50K/yr

Mentorship from experienced licensed inspectors * All licensing fees and materials covered ... Flexible work from home options available.

Home Inspector

Gorham, ME · On-site

$35K - $52K/yr

... Home inspection is a career most people don't know exists. You work independently, you're in a ... We pay you from day one to train alongside experienced inspectors, earn nationally recognized ...

Provide legal guidance during FDA inspections, investigations, and enforcement actions * Conduct ... ideally from a law firm or in-house setting * Demonstrated knowledge of CGMP and FDA regulatory ...

Drive to/from home inspections (insured personal vehicle required) * Perform complete exterior and interior property inspection according to company standards and industry standards of practice

Go from your home office to the jobsite each day. * Ongoing training and support * Tools and ... Home inspection is a moderately physical job Build Your Career in Home Inspection At NHI, you'll ...

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How do you become a from home FDA inspector?

To become a remote FDA inspector, candidates typically need a background in science, healthcare, or regulatory fields, along with relevant experience in inspections or compliance. Certification in areas such as food safety or pharmaceuticals can be beneficial, and strong analytical and communication skills are essential for conducting remote assessments and reporting findings.
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Infographic showing various From Home Fda Inspector job openings in the United States as of August 2026, with employment types broken down into 2% As Needed, 70% Full Time, 24% Part Time, and 4% Contract. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution.

Senior FDA Regulatory Attorney

The Rockridge Group

New York, NY • Remote

$250K - $350K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 16 days ago

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Job description

TITLE: FDA REGULATORY ATTORNEY

Firm X is seeking an experienced FDA Regulatory Attorney to join its growing FDA and Life Sciences practice. Due to significant client demand and a steady influx of new FDA-related matters, we are looking for an attorney with deep regulatory experience advising pharmaceutical, compounding, medical device, biotechnology, healthcare, and related life sciences clients.

Key Responsibilities:

  • Advise clients on FDA regulatory compliance matters involving drugs, biologics, medical devices, dietary supplements, and compounding pharmacies.
  • Counsel clients regarding FDA regulations, guidance, inspections, investigations, warning letters, and enforcement actions.
  • Provide guidance on:
    • Compounding (503A and 503B)
    • Drug Supply Chain Security Act (DSCSA)
    • cGMP compliance
    • Drug and device manufacturing requirements
    • FDA registrations and annual filings
    • Labeling, marketing, and advertising reviews
    • Product recalls and withdrawals
    • Import/export compliance
    • Veterinary medicine and veterinary compounding
  • Assist with NDA, ANDA, 510(k), PMA, OTC, and other FDA submissions.
  • Advise clients regarding clinical trial compliance, research agreements, informed consent forms, IRB requirements, and related regulatory matters.
  • Review scientific and clinical literature to support regulatory strategies and client guidance.

Qualifications:

  • J.D. from an accredited law school.
  • Licensed and in good standing in at least one U.S. jurisdiction.
  • 10+ years of FDA regulatory experience.
  • Prior law firm experience strongly preferred; exceptional in-house FDA counsel will also be considered.
  • Strong working knowledge of pharmaceutical, medical device, compounding, and healthcare regulatory frameworks.
  • Experience with FDA inspections, 483 responses, warning letters, and compliance programs preferred.
  • Clinical trial experience is a plus.
  • Patent and/or copyright filing experience is a plus.
  • Excellent drafting, analytical, and client counseling skills.

Company Description

About The Rockridge Group:

TRG is a privately held Limited Liability Company committed to connecting businesses with job seekers. We deliver high quality contingent personnel to our clients using our 3-step collaborative engagement model:
Collaborate. We partner with you to understand the unique needs of your business before we propose a solution.
Strategize. Based on your goals and staffing challenges, we develop high impact solutions designed for your industry.
Engage. We work with your team before, during, and after every engagement to deliver 100% satisfaction.
With over ten (10) years experience in the resource solutions sector, principals Greg Donner [link to bio] and Ronald Lom [link to bio] leverage the power of strategic partnership to create a powerful staffing model that improves your quality of hire.