Career Center

"Enhancing the Lives of Those We Touch by Helping People Reach Their Goals”

Melaleuca is a dynamic, high-growth $2B natural products company that manufactures and sells effective, high-quality, natural, health-oriented products. We are a feel-good lifestyle brand that is committed to changing lives. Melaleuca was created to provide our members with superior products that help people live more vibrant, healthier and happier lives. We are celebrating our 35th record setting year with our annual revenues in excess of $2 billion USD. We are expanding our operations and we are looking to add 2 auditors to our quality team!

The QA Auditor's will direct and conduct all quality audit activities both internally and externally (we have both an Internal and External Auditor position available). As such, outlines, originates, and performs audits at our facilities and with vendors to ensure compliance to company and regulatory guidelines.  Leads efforts in process improvements related to audit findings.

If you want to learn more, please apply.  We would love to have a conversation about your goals.

Responsibilities

• Coordinates audits of plant(s) and vendors for compliance to Federal Food, Drug, and Dietary Supplement GMP laws and internal procedures.
• Coordinates vendor audits to assess their ability to comply with company specifications and meet GMP requirements.
• Assists QA manager/director during FDA and other regulatory agency inspections.
• Coordinates the audit of documentation and recommends document changes for the plant.
• Researches possible causes and provides feedback regarding product quality issues raised by audits.
• Keeps current on regulatory actions in the Food, Drug, and Dietary Supplement industry.
• Writes internal and vendor audit reports.
• Works with vendors and purchasing to assure continuing conformance to specifications of incoming labels, components, ingredients, and outside-manufactured products.
• Keeps current on QA inspection results and procedures.
• Performs routine audits on historical batch records and other past OTC and DS documentation.
• Coordinates the yearly GMP awareness and compliance training. 

• CQA preferred but not required.
• Bachelor’s degree with 8 years manufacturing industry experience with at least 4 years experience with Quality Audits or working with vendors.
• A working knowledge of Federal Regulations regarding the manufacturing and distribution of drug products, Dietary Supplements and Foods
• Experience with FDA audits helpful.
• Self starter.