ZipRecruiter

Log In

1

Former Fda Jobs (NOW HIRING)

next page

Showing results 1-20

All JobsFormer Fda Jobs

Former Fda information

See salary details

$66.5K

$114.8K

$157K

How much do former fda jobs pay per year?

As of Jun 23, 2026, the average yearly pay for former fda in the United States is $114,766.00, according to ZipRecruiter salary data. Most workers in this role earn between $99,000.00 and $129,000.00 per year, depending on experience, location, and employer.

What is a Former FDA employee?

A Former FDA employee is an individual who previously worked for the U.S. Food and Drug Administration (FDA), an agency responsible for protecting public health by regulating food, drugs, medical devices, and other products. After leaving the FDA, these professionals may work in related industries, such as pharmaceuticals, consulting, or academia, often leveraging their regulatory expertise. Their insights and experience with FDA policies and procedures can be valuable for organizations seeking to navigate complex regulatory environments.

What are the key skills and qualifications needed to thrive as an FDA Regulatory Affairs Specialist, and why are they important?

To thrive as an FDA Regulatory Affairs Specialist, you need a strong background in life sciences, regulatory guidelines, and relevant experience in FDA submission processes, often supported by a bachelor's or advanced degree. Familiarity with regulatory databases, document management systems, and certifications like RAC (Regulatory Affairs Certification) are typically required. Excellent attention to detail, strong organizational skills, and effective communication are crucial soft skills for this role. These competencies ensure accurate compliance with complex regulations, successful product approvals, and protection of public health.

What are some typical challenges faced by professionals transitioning from an FDA regulatory role to positions in the private sector?

Professionals moving from the FDA to private sector roles often face the challenge of adapting from a regulatory, oversight-focused environment to one that emphasizes innovation and business growth. Navigating potential conflicts of interest, learning new company-specific processes, and balancing regulatory compliance with commercial objectives are common hurdles. However, their deep understanding of regulatory pathways and policy interpretation is highly valued, and many organizations provide onboarding support to ease this transition.
Subcontractor - Senior OTC Compliance Auditor (Great opportunity for former FDA Inspectors)

Subcontractor - Senior OTC Compliance Auditor (Great opportunity for former FDA Inspectors)

SGS

Remote

Full-time

Posted 20 days ago

Job description

Company Description
We are SGS - the world's leading testing, inspection and certification company. We are recognized as the global benchmark for sustainability, quality and integrity. Our 99,600 employees operate a network of 2,600 offices and laboratories, working together to enable a better, safer and more interconnected world.
Job Description
We are seeking a highly experienced Subcontractor - Senior OTC Compliance Auditor with a background as a former FDA Investigator/Inspector. This short-term assignment (May-August 2026) requires expertise in OTC drug manufacturing, cGMP compliance, and FDA inspection methodology.
As a subcontractor, you will support audits, inspection readiness activities, and compliance reviews for clients in the OTC pharmaceutical industry.
Key Responsibilities
  • Conduct cGMP compliance audits of OTC drug manufacturing, packaging, labeling, and laboratory operations.
  • Apply FDA inspection methodology to identify compliance gaps, risks, and deficiencies.
  • Prepare detailed, professional audit reports outlining observations and recommended corrective actions.
  • Support clients with mock FDA inspections, inspection readiness activities, and compliance remediation.
  • Review quality systems, SOPs, batch records, data integrity controls, and laboratory practices.
  • Represent the organization professionally during international client engagements.
  • Manage scheduling, travel, and deliverables independently as an external contractor

Qualifications
  • Former FDA Investigator/Inspector (required).
  • 3-5 years of auditing experience within OTC or pharmaceutical manufacturing.
  • Strong understanding of cGMP requirements, OTC monograph expectations, and FDA enforcement practices.
  • Proven ability to conduct independent, high-level audits and articulate findings clearly.
  • Excellent communication and technical writing skills.

Travel
  • Must be willing and able to travel internationally, outside of North America, for the duration of the contract.

Interested?
If you're a former FDA inspector with OTC auditing experience and open to a global contract assignment from May-August 2026, we'd like to connect.
Additional Information
SGS is an Equal Opportunity Employer, and as such we recruit, hire, train, and promote persons in all job classifications without regard to race, color, religion, sex, national origin, disability, age, marital status, sexual orientation, gender identity or expression and Indigenous status, or any other characteristics protected by law.
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily with or without reasonable accommodations. The requirements listed above are representative of the knowledge, skills, and/or abilities required.
This job description should not be construed as an exhaustive statement of duties, responsibilities, or requirements, but a general description of the job. Nothing contained herein restricts the company's rights to assign or reassign duties and responsibilities to this job at any time.
Accommodations are available on request for qualified candidates during each stage of the recruitment process.
Please note that candidates applying for Canadian job openings should be authorized to work in Canada

Apply