The role:
Work to provide a GMP compliance company .
Review equipment calibration and maintenance records to ensure they are performed correctly and on time.
Prepare and maintain Quality records for review of completeness and accuracy to meet both internal and external expectations during production run.
Perform Incoming component inspection
Collect samples from the packaging area for retains when needed.
Inspect filled product for expiration dates and lot/batch codes.
Assist with the actual labor and manufacturing of projects as time permits/ as needed.
Document nonconforming materials clearly and accurately with discrepancy reports, when required.
Ensure compliance with Company specific regulations related to the Quality of the product and the proper performance of day-to-day activities.
Reports any unusual quality incident to the Quality Supervisor in a timely manner.
Follow continual improvement practices and participate in cross-functional teams, which impact production, increase efficiency, solve problems, generate cost savings and improve quality.
Perform other duties as required.
Problem solver with a sense of urgency
High School Diploma or GED and 2 years manufacturing experience FDA regulated products.
Ability to communicate, math, write, and read in English.
Experienced with measuring instruments (scales, calipers, calibrating thermometers)
Basic computer literacy skills in Office Standard Microsoft Word, Excel and Google Office Suite
Schedule:Â 9:00pm - 5:30am
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