This is a 2nd Shift Position located in Cherry Hill, NJ.
The QA Coordinator schedules work performed by the analysts in the In-Process QA laboratory, responds to out-of-specification (OOS) results found by QA Analysts during in-process monitoring and reviews and approves documentation of the In-Process monitoring. The QA Coordinator also trains QA Analysts, maintains inventory and controls laboratory and controls laboratory supplies in accordance to department SOPs. When required, backs up the QA Supervisor in day-to-day activities. He/she is capable of covering the manufacturing floor in absence of QA Supervision and is also capable of issuing additional Batch record documents when needed by Operations or any other group. The person in this position is fully qualified to cover the floor as a QA Analyst in times of personnel shortage due to call outs or scheduled time-off.
Majority of the time is spent in review of paperwork and coordination of QA analyst activities. Has frequent contact with different areas of production and levels of management, in person or via email. Uses laboratory instrumentation, syringes, reagents and compressed gases on a daily basis.
Education and/or Experience:
Bachelors degree in Science or equivalent with >3 year applicable laboratory or pharmaceutical manufacturing experience (QA preferred).