Quality Assurance Manager

Ancient Nutrition

United States

Remote

USD 90,000 - 120,000

Full time

14 days+
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Job summary

A leading dietary supplement brand is seeking a Quality Assurance (QA) Manager to oversee quality systems, ensuring product quality, safety, and brand integrity across all manufacturers and suppliers. The role requires a Bachelor's degree in a relevant field and 6–10 years of QA experience, with strong knowledge of FDA regulations. This position allows remote work within the United States, excluding certain states. The ideal candidate will have excellent documentation skills and be a strategic thinker.

Qualifications

  • 6–10+ years of quality assurance experience in dietary supplements.
  • Experience working with contract manufacturers (CMOs).
  • Strong knowledge of FDA dietary supplement regulations.
  • Excellent documentation and technical writing skills.

Responsibilities

  • Communicate with manufacturers to ensure compliance with FDA regulations.
  • Manage SOPs, document control, and CAPAs.
  • Oversee customer complaint investigations and trending analysis.
  • Participate in recall readiness planning and mock recalls.

Skills

Quality Assurance
Regulatory Compliance
Technical Writing
Leadership
Communication

Education

Bachelor's degree in relevant field

Job description

We are seeking a highly experienced Quality Assurance (QA) Manager to lead and oversee quality systems for our growing dietary supplement brand. This role is responsible for ensuring product quality, safety, and brand integrity across all contract manufacturers, suppliers, and distribution partners.

As a brand-driven organization, quality is central to our reputation. The QA Manager will serve as the quality authority, ensuring our products meet FDA dietary supplement regulations (21 CFR Part 111 and 117), labeling requirements, and third-party certification standards while protecting consumer trust.

Key Responsibilities
Quality Oversight of Contract Manufacturers
  • Communicate with manufacturers (CMOs) to ensure compliance with 21 CFR Part 111 and 117 as well as cGMP requirements.
  • Review and approve Master Manufacturing Records (MMRs), Batch Production Records (BPRs), and Certificates of Analysis (COAs).
  • Complete and own finished product release and disposition decisions that do not require escalation.
Regulatory & Compliance
  • Maintain inspection readiness.
  • Oversee adverse event reporting and complaint investigations.
Documentation & Quality Systems
  • Utilize the company’s Quality Management System (QMS).
  • Manage SOPs, document control, change control, deviations, and CAPAs.
  • Participate in review and approval of finished product specifications.
  • Track quality metrics and prepare multi-level reporting.
Customer & Brand Protection
  • Oversee customer complaint investigations and trending analysis.
  • Participate in recall readiness planning and mock recalls in coordination with operations.
  • Protect brand integrity by proactively identifying quality risks.
Cross-Functional Collaboration
  • Partner with Product Development, Regulatory, Marketing, Supply Chain, and Operations teams to ensure quality is embedded from concept to commercialization.
  • Participate in cGMP and quality training to internal teams.
Qualifications
Education:
  • Bachelor’s degree in Food Science, Chemistry, Microbiology, Pharmaceutical Sciences, Regulatory Affairs, or related field.
Experience:
  • 6–10+ years of quality assurance experience in dietary supplements.
  • Experience working with contract manufacturers (CMOs).
  • Strong knowledge of FDA dietary supplement regulations (21 CFR Part 111, 117 & Part 101).
  • Experience with third-party certifications (e.g., NSF, USP, Non-GMO, Organic) preferred.
  • Strong understanding of brand protection and regulatory risk management.
  • Excellent documentation and technical writing skills.
  • Strategic thinker with the ability to balance compliance and business growth.
  • Strong communication and leadership abilities.
Key Performance Indicators (KPIs)
  • Timely batch release and deviation closure
  • Reduction in complaint trends
  • Monthly Quality and CMO data share
  • Ad hoc KPIs are requested

This position may be performed remotely within the United States where permitted by applicable law. At this time, we are not considering applicants residing in the following states: California, Colorado, New York, Washington, Oregon, New Jersey, Minnesota, Massachusetts, Maine, Wisconsin, Pennsylvania, or Ohio.

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