Production Associate O1 (SVLM) 3rd Shift, Sun - Thurs, 10:00pm - 6:30am

Role responsibilities

The role involves following work policies and procedures to perform quality control inspections and production tasks within a GMP environment. Responsibilities include reporting compliance concerns and ensuring products conform to specifications through proper documentation.

Requirements

Candidates must have a High School Diploma or GED and the physical ability to lift up to 50 lbs and work in an ISO5 clean room environment. Previous manufacturing experience and proficiency in MS Office are considered a plus.

Key skills

GMP, Good Documentation Practices, Quality Control Inspection, EHS Compliance, Clean Room Gowning, MS Office, Production Process Knowledge, Material Identification & Segregation

Keywords

GMP, ISO5, Life Sciences, Biotechnology, Quality Control, Clean Room, PPE, Small Volume Liquid Media, Danaher Business System, Manufacturing, EHS, Documentation Configuration Control, Non-conforming Documentation, Rework Documentation