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Why Join New Generation Wellness  

As we approach our centennial milestone, New Generation Wellness is celebrating more than 100 years of commitment to health, quality, and innovation. Our longevity reflects a stable, science-driven organization where Quality plays a critical role in protecting consumers and enabling responsible growth. 

At NGW, Quality Assurance is empowered, respected, and embedded in decision-making. This role offers hands-on leadership, strong cross-functional partnership, and a clear path into senior Quality leadership. 

Position Summary: 

The Quality Assurance Supervisor provides daily leadership and oversight of Quality Assurance activities supporting manufacturing, packaging, and quarantine operations in a cGMP-regulated environment. This role ensures compliance with FDA regulations, internal SOPs, and quality-system requirements while fostering a proactive, collaborative quality culture. 

Reporting to the Quality Manager, the QA Supervisor leads and mentors QA staff, supports audit readiness, drives documentation accuracy, and partners closely with Operations and Product Development to ensure product quality and regulatory compliance. 

This is an ideal opportunity for a hands-on QA professional ready to expand their leadership impact while maintaining direct involvement in quality systems and floor-level execution. 

Key Responsibilities 

QA Leadership & Daily Oversight 

• Supervise day-to-day QA activities across manufacturing, packaging, and quarantine operations 

• Lead, train, and mentor QA Technicians, providing coaching, performance feedback, and scheduling support 

• Serve as a visible quality presence on the production floor 

• Exercise authority—with organizational support—to stop production or withhold product release when quality or compliance risks are identified 

Quality Systems & Compliance 

• Support equipment qualifications (IQ/OQ) and cleaning validation activities 

• Partner with Supplier Quality to support raw-material and vendor qualification processes 

• Review batch records and oversee documentation accuracy and completeness 

• Coordinate deviation investigations, nonconformance documentation, and CAPA activities 

• Support root-cause analysis and track CAPA effectiveness 

• Manage change-control documentation to ensure traceability and regulatory alignment 

• Track and trend quality metrics and report findings to Quality leadership 

Training & Technical Support 

• Coordinate QA-related training programs in collaboration with HR and department leaders 

• Ensure training records are current and aligned with role-specific competencies 

• Act as a technical resource and mentor for QA Technicians 

Auditing & Inspection Readiness 

• Participate in internal and external audits, serving as a subject matter expert 

• Support preparation for FDA and customer inspections 

• Monitor and follow up on corrective actions resulting from audit findings 

Cross-Functional Collaboration & Continuous Improvement 

• Partner with Manufacturing, Product Development, and Supply Chain to support compliant, efficient operations 

• Participate in quality review boards and continuous improvement initiatives 

• Identify opportunities to improve documentation flow, approval timelines, and QA processes 

• Support enhancements to electronic Quality Management Systems (QMS) 

Success Measures 

• Accuracy and timeliness of batch record and document reviews 

• Deviation and CAPA closure effectiveness 

• Audit readiness and inspection outcomes 

• Training completion and team development progress 

• Contributions to quality culture and process improvement initiatives 

Qualifications 

Education 

• Bachelor’s degree in a scientific or technical discipline (Biology, Chemistry, Food Science, or similar) preferred 

• Equivalent regulated-industry experience will be considered 

Experience 

• 4–6 years of Quality Assurance experience in a regulated manufacturing environment (dietary supplements, nutraceuticals, pharmaceuticals, food, or similar FDA-regulated industry) 

• 1–2 years of experience in a lead or supervisory capacity preferred 

• Hands-on experience with batch record review, deviation investigations, CAPA management, and internal audits 

Knowledge & Skills 

• Strong working knowledge of cGMPs, FDA regulations, and Good Documentation Practices (GDP) 

• Experience working with ERP systems and electronic QMS platforms 

• Strong analytical, organizational, and technical writing skills 

• Ability to lead, mentor, and influence others in a fast-paced manufacturing environment 

• Detail-oriented, accountable, and comfortable making quality-driven decisions 

Work Environment & Physical Requirements 

• Primarily office-based with regular time spent in manufacturing areas 

• Requires extended periods of computer work and walking the production floor 

• Occasional lifting up to 20 lbs 

• Use of PPE including lab coat, hairnet, safety glasses, and hearing protection as required 

Career Growth 

NGW is committed to developing Quality leaders. This role offers a defined progression path: 

Director of Quality 

Quality Manager  

Quality Assurance Supervisor 

Advancement is supported through leadership exposure, system ownership, and cross-functional collaboration.