QUALITY ASSURANCE TECHNICIAN

POSITION SUMMARY The Quality Assurance Technician works independently and coordinates essential Quality Assurance / Quality Control functions, from raw materials and current Good Manufacturing Practices (cGMPs) verification through finished product release. This includes quality control of manufacturing processes. Nutiva employees are expected to embrace Nutiva’s four values of Passion, Purity, Community, and Well-Being. These values guide our team in representing Nutiva to our associates, vendors, and customers. MAJOR RESPONSIBILITIES Perform component or product inspection, sampling, analyses following standard methods and procedures, and approval/release. Incorporate or develop new procedures as needed. Evaluate the validity of test data received/obtained. Review data for conformance to specifications. Record test data, enter data into computer, and generate Certificates of Analyses. Maintain equipment, records (logs, documentation, calibration, etc.), laboratory area, and retention samples in compliance with regulatory guidelines and company procedures (cGLPs, cGMPs, SOPs). Maintain adequate inventory levels of laboratory supplies and/or supplies needed for QA activities at contract manufacturing locations (identify, purchase, etc.). Develop, adhere to, and improve laboratory safety procedures. Ensure compliance with Laboratory Hazardous Waste Generator regulations and manage related documentation. Inspect and/or audit manufacturing processes, records, or products, emphasizing adherence to cGMP standards. Interpret and enforce Nutiva QA/QC standards to ensure product quality. Participate in experiment design and execution, applying scientific judgment with accuracy. Liaise with outside entities (contract manufacturers, laboratory equipment vendors, etc.). Conduct QA production line inspections and cGMP checks. Inspect, review, test, approve, reject, and disposition incoming components, WIP, or finished goods. Maintain QA documentation and records, both physical and electronic. Sample and maintain QA retention samples. Conduct in-house QA analyses, including laboratory tests, sensory evaluations, visual inspections, etc. Prepare samples for third-party laboratory analysis as needed. Assume additional responsibilities as assigned. QUALIFICATIONS Position-Specific Skills Required Minimum of 3-5 years practical experience in a quality, laboratory, or cGMP regulated production environment in 21 CFR regulated industries (food, dietary supplements, personal care, medical devices, etc.). Excellent written and verbal communication, analytical, and problem-solving skills. Good interpersonal skills to function effectively as part of an interdisciplinary team. Strong organizational skills with attention to detail. Technical Skills Required Knowledge of cGMPs, HACCP/food safety, laboratory safety, GFSI/SQF, ISO, National Organic Program, and Kosher guidelines is a plus. Proficiency with Microsoft Windows or Apple operating systems and applications, including Microsoft Office Suite (Word, Excel, PowerPoint). Experience with relational databases and tools for data interpretation. Experience working with version-controlled forms, procedures, policies, and workflows. Education/Training Required Four-year college degree in a technical/scientific discipline (Food, Physical, or Biological Sciences preferred). Work Environment and Physical Demands Sitting 30%; Walking 30%; Standing 40%. Frequently lift/move up to 10 lbs., occasionally up to 25 lbs. Exposure to manufacturing equipment hazards. Some travel required. About Us Nutiva is an innovative leader in the organic food industry, known for organic coconut, hemp, chia, and red palm superfoods. We are committed to nourishing people and the planet, donating 1% of sales to sustainable agriculture. Named one of the fastest-growing private companies in America by Inc. Magazine, Nutiva offers a fast-paced, dynamic environment where we aim to revolutionize the way the world eats.

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