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

Role overview

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
  • Excellent communication and technical writing skills

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

Key facts

  • Remote from: United States
  • Full time
  • Senior (5-10 years)
  • Compliance Analyst
  • English

Hard skills

Other skills

  • Communication
  • Problem Solving

About the company

SGS  logo

SGS

Audit & Assurance Services

We are SGS – the world’s leading testing, inspection and certification company. We are recognized as the global benchmark for quality and integrity. Our 96,000 employees operate a network of 2,600 offices and laboratories, working together to enable a better, safer and more interconnected world. Community Guidelines Welcome to our LinkedIn page! SGS encourages all fans of this page to participate in the conversation through questions and comments. Any comments or activity arising from persons sharing or otherwise reproducing any communications published by SGS is not controlled or endorsed by SGS. We want to promote an informative and enjoyable environment within this community; we therefore ask that you post content that is both relevant and respectful and that you follow LinkedIn's Professional Community Guidelines; https://help.linkedin.com/app/answers/detail/a_id/34593/~/linkedin-professional-community-guidelines Posts will be removed if they are: - Offensive, defamatory, discriminatory or obscene - Fraudulent, deceptive or misleading - In violation of any intellectual property rights - In violation of any law or regulation - Abusive, harassing, stalking, threatening or attacking others - Trolling or deliberate disruption of discussion - Commercial solicitations or personal promotion - Spam, link baiting or files containing viruses that could damage the operation of other people’s computers or mobile devices

Company details

Company typeLarge
IndustryAudit & Assurance Services
Company size10001

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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, 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

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MR

Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
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