PSG Global Solutions
QC Associate II/III
PSG Global Solutions, Fremont, California, us, 94537
DescriptionWe're looking for a
QC Associate II/III , working in
Pharmaceuticals
and
Medical Products
industry in
6397 Kaiser Drive, Fremont, California, 94555, United States .
Job description:
Executes routine and non-routine testing operations in QC of bulk drug substance and drug product in a multi-product facility.Performs duties under limited supervision and according to standard operating QC procedures.Executes independently with adequate training fundamental operations such as HPLC and Capillary electrophoresis.Performs internal support duties including stocking consumables/materials, updating controlled SOP binders, appropriately discarding expired reagents, recognizing and reporting process and equipment anomalies.Delivery of high quality analytical results within timeline right the first time.Documents work according to cGMP and cGDP.Adheres to established regulations and follows cGMP established by site.Reports abnormalities and deviations in a timely and accurate manner.Adheres to safety standards and identifies unsafe situations/ habits and escalates appropriately.Maintains work production areas according to predefined standard (5s).
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QC Associate II/III , working in
Pharmaceuticals
and
Medical Products
industry in
6397 Kaiser Drive, Fremont, California, 94555, United States .
Job description:
Executes routine and non-routine testing operations in QC of bulk drug substance and drug product in a multi-product facility.Performs duties under limited supervision and according to standard operating QC procedures.Executes independently with adequate training fundamental operations such as HPLC and Capillary electrophoresis.Performs internal support duties including stocking consumables/materials, updating controlled SOP binders, appropriately discarding expired reagents, recognizing and reporting process and equipment anomalies.Delivery of high quality analytical results within timeline right the first time.Documents work according to cGMP and cGDP.Adheres to established regulations and follows cGMP established by site.Reports abnormalities and deviations in a timely and accurate manner.Adheres to safety standards and identifies unsafe situations/ habits and escalates appropriately.Maintains work production areas according to predefined standard (5s).
#J-18808-Ljbffr