Quality Inspector I 3rd shift

Herbalife•Winston-Salem, NC

1d•Onsite

About The Position

The 3rd Shift MQA Technician I is responsible for conducting quality control checks of materials, products, and documentation before, during, and after batch production activities. This role involves performing pre-batch inspection activities, swabbing of equipment to verify cleanliness, in-process quality control checks for low-speed Powder and Tea packaging lines, and ensuring batch-related documentation is completed accurately and completely in real-time. The technician will also manage the status of production materials and detail quality-related incidents using appropriate GMP documentation.

Requirements

Attention to detail
Good interpersonal and communication skills
Ability to communicate effectively verbally and in written English
Digital 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 the pressure of manufacturing
Must be able to operate a motorized powered lift i.e. Forklift, Scissor lift, one man lift, etc. A MVR (Motor Vehicle Report) will resolve an employee’s eligibility to operate these lifts.
A minimum of 1 year of experience in FDA or GMP regulated industry
High-school diploma (equivalent)

Nice To Haves

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

Responsibilities

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 lines
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 the status of production materials to released, rejected, hold, etc.
Detail 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 management
Performs other related duties as assigned by management.