Technician II, Manufacturing Quality Assurance

Overview

Position Summary Statement:
The MQA Technician II is responsible for conducting quality control checks of materials, products and documentation before, during and after batch production activities. They are also responsible for conducting sensory, physical and chemical testing of in‑process materials to verify they meet specifications.

• Perform pre‑batch inspection activities (e.g., verify line clearance, review staged materials, review batch‑related documentation, inspect initial units, line release, etc.), swab equipment to verify cleanliness before use, and conduct in‑process quality control checks for low‑ and high‑speed Powder and Tea packaging lines and Liquid packaging line.
• Perform sensory, physical and/or chemical analysis of in‑process materials to confirm they meet specifications.
• Assist production staff with correct understanding and implementation of GMP procedures and company policy.
• Document and investigate foreign materials and metal discovered during manufacturing and packaging activities.
• Perform swabbing of manufacturing equipment to verify cleanliness.
• Perform in‑process quality control checks.
• Ensure batch‑related documentation is completed accurately and completely in real‑time.
• Change status of production materials to released, rejected, hold, etc.
• Document quality‑related incidents using appropriate GMP documentation (e.g., nonconforming materials report, unplanned deviation report, quality incident report).
• Review production‑related GMP documentation (e.g., production logbooks) to ensure they are being completed accurately and completely.
• Report any violations of GMP procedures or company policy to MQA management.
• Perform other related duties as assigned by management.

• Attention to detail.
• Good interpersonal and communication skills.
• Ability to communicate effectively verbally and in written English.
• Computer literacy, with solid PC and software experience.
• Ability to lift a minimum of 30 lbs.
• Strong ability to work independently and as a team member under pressure of manufacturing.
• Position requires operation of a motorized powered lift (e.g., forklift, scissor lift, one‑man lift, etc.). A MVR (Motor Vehicle Report) will determine eligibility to operate lifts.

• Minimum of 2 years of experience in FDA or GMP regulated industry.

• High‑school diploma (or equivalent).

• Experience with food, supplement or pharmaceutical manufacturing.
• Knowledge and understanding of GMP quality systems.

Herbalife offers a variety of benefits to eligible employees in the U.S. (limited to the 50 States and the District of Columbia), including Group Health Programs, other Voluntary Benefit Programs, and Paid Time Off. Group Health Programs include Medical, Dental, Vision, Health Savings Account (HSA), Flexible Spending Accounts (FSA), Basic Life/AD&D;
Short‑Term and Long‑Term Disability, and an Employee Assistance Program (EAP). Other Voluntary Benefit Programs include a 401(k) plan, Wellness Incentive Program, Employee Stock Purchase Plan (ESPP), Supplemental Life/Critical Illness/Hospitalization/Accident Insurance, and Pet Insurance. Paid time off includes Company‑observed U.S. Holidays, Floating Holidays, Vacation, Sick Time, a Volunteer Program, Paid Maternity and Paternity Leave, Bereavement Leave, Personal Leave and time off for voting.