St. Louis $30.00 - $32.00 p/h Contract
Reviewing and approving batch records
Conducting AQL inspections
Performing clearances for manufacturing areas
Providing quality input and guidance to manufacturing personnel
Dispositioning finished product, raw materials, and components
Releasing incoming raw materials and components
Maintaining quality records
Investigating quality issues
Developing and implementing quality improvement initiatives
Bachelor Degree preferred in life science or a related field; or equivalent experience.
Six or more years of relevant quality/quality control/production experience in a cGMP facility.
Excellent attention to detail skillset.
Experience with computer data entry required. Proficient in use of Microsoft suite office products.