Quality Specialist

Description Who We Are Looking For We are looking for a detail-oriented quality professional to join our team as a n entry-level q uality s pecialist within our QA department. In this role, you will manage complex quality-related tasks, lead and facilitate out-of-specification investigations, and partner with cross-functional teams in project meetings and technical reviews to resolve quality issues and support operational goals. You'll be recognized for accuracy, sound judgment, and a commitment to regulatory and quality standards, while sharing knowledge and driving continuous process improvements that support USANA's mission of delivering high-quality products.   What You Will Do as USANA's Quality Specialist  •           Develop, implement, and maintain quality assurance systems and processes in alignment with cGMP, FDA, and international regulations •           Write, edit, review, and implement controlled documents; maintain accurate and complete records, including historical and GMP files; and prepare trend reports and presentations •           Participate in and support internal quality audits, including audit preparation, execution assistance, responses, and follow-up activities •           Support the stability program through documentation, data review, trending, and compliance activities in accordance with regulatory requirements •           Assist in risk assessment meetings and processes, including supplier and raw material risk evaluations •           Investigate and resolve product and process quality issues, support customer complaint investigations, and assist with operational and quality deviations and non-conformance investigations •           Ensure adherence to regulatory, safety, and company policies, and maintain knowledge of government and industry QA codes and standards •           Perform other duties as assigned to support quality and business objectives   Background and Skills You Will Need •           Bachelor's degree in c hemistry, b iology, p harmaceutical s ciences, or a related field •           One to two years of experience in quality assurance, document control, or compliance within the dietary supplement, pharmaceutical, or personal care industries •           Detail-oriented with strong organizational and recordkeeping skills •           Ability to manage multiple documentation tasks and meet deadlines •           Proficiency with Microsoft Office and document management software •           Effective written and verbal communication skills •           Strong team collaboration and a willingness to learn   What Will Make You Standout •           Experience with QMS documentation or electronic quality management systems •           Familiarity with FDA 21 CFR 111/211, cGMP, and ISO standards, and a basic understanding of cGMP and quality system principles   This is a hybrid remote role with regular weekly in-office time in Salt Lake City.    Who We…