Quality Assurance Coordinator

Isagenix•Gilbert, AZ

3d•Hybrid

About The Position

This position is responsible for executing and performing multiple cross-functional activities within Isagenix Quality Assurance program which includes functions in document control, quality control, quality assurance incoming product inspections and approvals, as well as product complaints. The position would provide management with briefings and timely reports reflecting the status of documents within a new document control system relevant to current documentation, actively participate in incoming quality assurance inspections, approvals, and rejections, as well as assisting with complaint monitoring and reporting. Work Schedule: This position currently follows a hybrid work model. Employees are required to work from the office at least four days per week (Monday - Thursday), with Friday available for remote work, offering a blend of in-person collaboration and flexibility. Established in 2002, Isagenix International has created simple, proven products that optimize what your body is capable of—helping you protect your greatest asset, your health. For more than twenty years, Isagenix has made holistic science an art with transparency and integrity—creating products and systems that address nutrition, stress, fitness, energy, natural beauty, focus, and financial wellbeing. The global wellbeing company, based in Gilbert, Arizona, markets its products through a network of independent distributors in 22 key markets: the United States, Canada, Puerto Rico, Australia, New Zealand, Mexico, the United Kingdom, Ireland, the Netherlands, Belgium, Spain, Austria, Denmark, Finland, France, Germany, Italy, Norway, Poland, Portugal, Sweden, and Switzerland. For more information, visit Isagenix.com.

Requirements

Associate’s degree in a fundamental science from an accredited institution or equivalent related experience.
1 year of analytical food laboratory experience.
Knowledge of dietary supplement and food testing methods.
No dietary restrictions or allergies.

Responsibilities

Actively work within the Isagenix Quality Management System (QMS), QualityOne, to support the quality functions in an efficient manner.
Create, review, and revise Isagenix required documentation to ensure compliance to market regulations: FDA 21 CFR 111, 117, and others as applicable.
Escalate any new, unknown product risks or hazards for further evaluation and decisions.
Assist in coordinating and processing finished product master documents for external communication.
Assist with creating, revising, and reviewing SOPs, Process Flow Charts, and other controlled documents.
Track projects, provide updates and provide status reports, as required by management or QA procedures.
Assist with organoleptic evaluations for product qualifications, release samples, shelf-life study samples and taste testing, as needed.
Assist with collecting, reviewing, and organizing information for finished product specifications including analysis of testing methodologies.
Assist with processing laboratory results, data collections, statistical evaluations, trend and prepare quality control reports based on results and data.
Process, coordinate and track internal sample processing and sample submissions to contract laboratories.
Maintain logs (laboratory, tracking, inventory, etc.) and analytical data in an organized, secure manner.
Expand scope of Quality Control by identifying opportunities for improvement and solutions.
May represent QA at company commercialization (POD) meetings, providing status updates on new products and relay all pertinent information to QA team, as needed.
Support other areas or individuals within the Quality department as needed.