Technician I, Manufacturing Quality Assurance (3rd shift Sunday night- Friday morning 10pm-6:30am)

OverviewPOSITION SUMMARY STATEMENT:The MQA Technician I is responsible for conducting quality control checks of materials, products and documentation before, during and after batch production activities.DETAILED RESPONSIBILITIES/DUTIES:Perform pre-batch inspection activities (e.g., verify line clearance, review of staged materials, review of batch-related documentation, inspection of initial units, line release, etc.), swabbing of equipment to verify cleanliness before use, and in-process quality control checks for low-speed Powder and Tea packaging linesPerform swabbing of manufacturing equipment to verify cleanlinessPerform in-process quality control checksEnsure batch-related documentation is completed accurately and completely in real-timeChange the 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, etc.)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 managementPerforms other related duties as assigned by management.!SUPERVISORY RESPONSIBILITIES:NoneQualificationsREQUIRED QUALIFICATIONS:Skills:Attention to detailGood interpersonal and communication skillsAbility to communicate effectively verbally and in written EnglishDigital literacy, with solid PC and software experienceAbility to lift a minimum of 30 lbsStrong ability to work independently and as a team member under the pressure of manufacturingThis position will require the employee to operate a motorized powered lift i.e. Forklift, Scissor lift, one man lift, etc. A MVR (Motor Vehicle Report) will determine an employee’s eligibility to operate these lifts.Experience:A minimum of 1 year of experience in FDA or GMP regulated industryEducation:High-school diploma (or equivalent)PREFERRED QUALIFICATIONS:Experience with food, supplement or pharmaceutical manufacturingKnowledge and understanding of GMP quality systemsAt Herbalife, we value doing what’s right. We are proud to be an equal opportunity employer, making decisions without regard to race, color, religion, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability, or any other protected characteristic. We value diversity, strive for inclusivity, and believe the differences among our teammates is a key contributor to Herbalife’s ongoing success.Herbalife offers a variety of benefits to eligible employees in the U.S. (limited to the 50 States and the District of Columbia), which includes 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.If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please email your request to [email protected].Terms of Use Privacy Policy CCPA Supplemental Notice Herbalife Consumer Health Data Privacy Policy