3–5 years of Quality Assurance (QA) experience in food, beverage, ingredients, dietary supplements, or nutraceutical manufacturing, including contract manufacturing / co-packing.
Experience with CMOs, co-packers, or ingredient suppliers, including private label and contract manufacturing organizations.
Proven expertise in company and supplier quality management, supplier qualification, and product approvals.
Strong understanding ofFDA regulations, dietary ingredient and beverage requirements, HACCP, HARPC, and general quality compliance standards.
Working knowledge of FSMA, including FSVP / FSVA.
Technical documentation expertise, including:
SDS (Safety Data Sheets)
Specifications
Allergen / GMO statements
BSE/TSE letters
Nutritional data
Test methods
Certifications
Supplier Ingredient Data Information (SIDIs)
PCQI certification (or willingness to obtain). QA experience with product release a plus.
Proficiency in Microsoft Excel, Word, and Outlook.
Experience with QMS/CRM systems (Salesforce, Compliance Quest preferred).
Review and assess supplier-provided technical documents for raw materials and finished goods, including SDSs, specifications, allergen/GMO statements, BSE/TSE letters, nutritional data, test methods, certifications, and SIDIs.
Lead product and supplier approval processes, ensuring compliance with internal SOPs, regulatory standards, and customer expectations.
Partner with co-packers, CMOs, and ingredient suppliers to gather updated documentation and evaluate change notifications.
Manage change control workflows, ensuring timely and accurate communication across internal and external stakeholders.
Respond to customer documentation requests related to ingredients, products, beverages, and manufacturing facilities.
Confirm alignment between customer and supplier specifications for product approvals, orders, and custom requests.
Oversee product release, ensuring all items meet testing, documentation, and quality standards before distribution.
Maintain and upload current technical data and quality documentation in ComplianceQuest.
Support sample management processes, including storage, tracking, and outgoing shipments with proper documentation.
Perform additional duties as assigned by Quality leadership (Associate Director or Vice President of Quality).
With extensive scientific, clinical, and healthcare industry experience, Joulé recruiters excel at placing talent across core specialty areas:
Working across every scientific discipline, Joulé places biologists, chemists, scientists, technicians and other specialists.
From research to regulations, safety to statistics, Joulé helps clients manage every stage of the clinical development lifecycle.
Laboratory and facility support comes with a total quality commitment backed by ISO 9001:2008 certification.
Trust Joulé’s extensive experience in physician, advanced practice provider and executive direct placement search.