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Job Description
Quality Assurance & GMP Compliance Manger
NUTRILAB LLC
Miami, FL Job Details Part-time | Full-time $50,518.38 - $80,839.34 a year 6 hours ago Qualifications GMP Manufacturing facility HACCP Attention to detail FDA regulations Full Job Description Overview We are seeking a dynamic and detail-oriented Quality Assurance & GMP Compliance Manager to lead our quality management initiatives and ensure strict adherence to Good Manufacturing Practices (GMP) and regulatory standards. In this pivotal role, you will champion the development, implementation, and continuous improvement of quality systems across manufacturing operations. Your expertise will help maintain product integrity, safety, and compliance with industry standards such as FDA dietary supplement regulations, HACCP, ISO 9001, NSF/ANSI 455, and other relevant frameworks. Join us to drive excellence in quality assurance and uphold the highest standards of manufacturing integrity. Duties Develop, implement, and oversee comprehensive quality management systems aligned with
FDA 21 CFR
Part 111, ISO 9001, NSF/ANSI 455, and GMP requirements. Conduct regular quality audits across manufacturing facilities to verify compliance with internal policies and external regulatory standards. Lead investigations into quality issues, non-conformances, deviations, and customer complaints; coordinate corrective and preventive actions (CAPA) to resolve issues effectively. Ensure all manufacturing processes adhere to GMP requirements, HACCP principles, and applicable dietary supplement regulations. Manage documentation related to quality inspections, specifications, validation protocols, calibration records, batch production records, and audit reports to maintain audit readiness. Facilitate training programs for staff on quality systems, GMP compliance, QA/QC procedures, documentation practices, and regulatory updates. Collaborate with cross-functional teams on new product development projects to embed quality assurance from formulation through production. Skills Extensive knowledge of FDA dietary supplement regulations (21 CFR Part 111), HACCP principles, cGMP standards, NSF/ANSI 455 requirements, and
ISO 9001.
Proven experience conducting quality audits and inspections within manufacturing environments. Strong understanding of quality control (QC), quality assurance (QA), supplier qualification programs, specifications management, and overall quality management systems (QMS). Excellent analysis skills for root cause analysis and data-driven decision making in a regulated environment. Project management capabilities to lead continuous improvement initiatives effectively. Effective communication skills for training staff and collaborating with regulatory agencies, auditors, suppliers, and manufacturing teams. Demonstrated ability to interpret technical documentation and implement compliance strategies across diverse teams. Join us in shaping a culture of excellence where your expertise ensures our products meet the highest safety, quality, and regulatory standards.
