About this role
With a legacy spanning more than 80 years, NSF leverages science and innovation to improve human and planet health. We provide science-driven, independent testing, inspection, certification, and advisory services and develop the very standards that drive the food, water, and life sciences industries worldwide. We empower our clients to navigate shifting regulations to improve consumer health, safety, and quality of life.
One of our core values is We Are One NSF. This means that while we’re one team, we embrace the cultural, ethnic, language, and demographic diversity that reflects the societies in which we live and work.
Come join a team that makes a difference in the world. More information about NSF can be found at nsf.org.
NSF is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to, among other things, race, color, religion, sex, sexual orientation, gender identity, national origin, age, status as a protected veteran, or disability.
Notice to Agency and Search Firm Representatives: Please note that NSF is not accepting unsolicited resumes from agencies/search firms for this role. Resumes submitted to an NSF employee by a third-party agency without a valid written & signed search agreement between NSF and said third-party agency will become the sole property of NSF. No fee will be paid if a candidate is hired as a result of an unsolicited agency or search firm referral. Thank you.
The Dietary supplement Auditor II – Product Certification is responsible for conducting product certification audits in accordance with applicable certification program requirements as assigned, regulatory standards, and accreditation rules, including but not limited to NSF/ANSI 455 Standards for Dietary Supplements, Cosmetics, and OTC Drugs. The Auditor II performs audits independently, evaluates implemented quality and product safety systems using objective evidence, and prepares clear, defensible audit reports that meet certification and accreditation expectations.
Audit Execution
• Conduct initial, surveillance, and special product certification audits for regulated consumer products, including dietary supplements, cosmetics, and OTC drugs • Perform audits in accordance with applicable certification program requirements as assigned, regulatory standards, and accreditation rules, including but not limited to NSF/ANSI 455 Standards (Dietary Supplements, Cosmetics, OTC Drugs) • Evaluate implemented and documented systems using objective evidence observed during the audit • Verify compliance with applicable standards, regulations, and program requirements within assigned audit scope • Conduct special visits related to complaints, product failures, enforcement actions, or verification of corrective actions Audit Reporting
• Prepare accurate, objective, and evidence‑based audit reports that: • Reflect only activities, records, and conditions observed during the audit • Clearly document conformity and nonconformity against auditable requirements • Exclude consulting, advisory, or future‑based language
• Write nonconformances that are clear, stand‑alone, and defensible to independent technical review Professional Conduct and Communication
• Maintain effective communication with certification management, technical reviewers, and project teams • Represent the certification body professionally during audits and client interactions • Identify systemic risks, recurring issues, or areas requiring escalation in accordance with certification and accreditation procedures Qualification and Competence Maintenance
• Obtain and maintain, as applicable, auditor qualification and authorization status as required by assigned certification programs and accreditation rules • Participate in required training, assessments, and evaluations to demonstrate and maintain technical competence • Complete periodic reassessments or witness evaluations when required by program or accreditation expectations • Maintain sufficient audit activity or supporting evidence to demonstrate ongoing competence
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Education
• Bachelor’s degree in a scientific, technical, regulatory, or quality‑related discipline • Alternative degrees may be accepted when supported by documented relevance to product safety, quality systems, or regulatory compliance Experience
• Minimum two (2) years of relevant experience in one or more of the following: • Quality systems • Manufacturing operations • Regulatory compliance • Product safety or quality assurance
• Experience with dietary supplements, cosmetics, OTC drugs, or other regulated consumer products preferred Technical Knowledge & Training
• Lead Auditor training or equivalent • Working knowledge of: • GMP‑based quality systems • Risk‑based auditing principles • Applicable regulatory and certification frameworks, including NSF/ANSI 455 Standards, as applicable to assigned scope
• Ability to complete additional program‑specific training as required to meet minimum qualification expectations Skills & Attributes
• Strong analytical and critical‑thinking skills • Clear, precise technical writing ability • Sound professional judgment aligned with accreditation expectations • Ability to work independently from a remote/home‑based location • Willingness and ability to travel as required Other Requirements
• Valid driver’s license and reliable transportation • Proficiency with Microsoft Word, Excel, Outlook, and electronic audit and reporting systems