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Job Summary & Purpose:
The main responsibility of a Quality Control Agent is to inspect and quality-check all PureBulk products before, during, and after the manufacturing process. This position works closely with the customer service and production department to assist customers with COA’s, shipping, and final product discrepancies. This position also supports the QU Manager with any quality control issues within PureBulk, Inc.
Duties and Responsibilities:
Perform quality checks on all PureBulk products throughout the production process.
Create MBR’s (manufacturing batch records) for production and provide all relevant documentation.
Review relevant documentation, provide certificates-of-analysis, MSDS/SDS, and sign off all drums for shipment to customers.
Review production functions as a Quality Control agent.
Support manufacturing by troubleshooting and helping to resolve internal out-of-specification processes and conditions with the support from the Quality Unit Manager.
Support manufacturing with selecting the right batch of raw materials for production.
Support the QU Manager during the investigations for any non-conformances.
Support QU Manager on updating revisions of labels in the label books and index.
Communicate with Operations Manager regarding MBR request sheets for upcoming weeks and quantities.
Maintain reference sheets such as botanicals, allergens, spoon charts, etc.
Participate in safety committee
Maintain FTIR QA intake forms, bulk densities, and pending new labels paperwork.
Receive incoming shipments (raw materials).
Run sampling sessions on raw material, prepare the sample bags and paperwork, and communicate with Operations Manager regarding any sampling sessions that QC needs their assistance with.
Update and log commercial sales in the COA tracking log.
Log returns in the customer service log and disperse returns to the appropriate person (Operations Manager, QA Lead)
Move released micros to the receiving area
Perform weekly internal audits including clean room, wet room, and warehouse.
Perform weekly water testing in the wet room.
Customer Service backup for answering phones.
Collect daily micros from the cleanroom and fill out the form and deliver it to Customer Service for mailing.
Support the QU Manager in quality checking labels and delivering to the cleanroom.
Assist with other duties as assigned by the manager.
Qualifications:
GED/Diploma or equivalent education or training with approval from the Director.
Experience with FDA/cGMP compliance is preferred
Knowledge of MS Word, Excel, database management.
Strong interpersonal, written, and oral communication skills.
Effectively organize and manage work responsibilities with minimal supervision.
Ability to multi-task and prioritize is essential.
Working Conditions & Physical Demands:
Long hours on the computer with typing and data entry. (Use of wrist and motor skills)
Lifting/Carrying/Pulling/Pushing/Kneeling/Bending: Frequently – Most tasks in the warehouse require lifting drums and boxes, carrying tubs, pulling, and pushing of carts and micro shelves. The typical weight range is 10-50 lbs.
Work is performed indoors in an office environment and in a production environment with exposure to noise, dust from products, cleaning agents.
Must adhere to company safety policies and cGMP policies. Wear the required personal protective equipment and clothing.
Requires the ability to communicate effectively using speech, vision, and hearing.
Email Resume to [email protected]
Vacancy caducado!