QC Associate II/III

Fremont, CA Contract Duration: 12-36 months Rate: Negotiable Salary: NA, $1.00 Responsibilities: Excellent employment opportunity for a QC Associate II/III in the Fremont, CA area. Execute routine and non-routine testing operations in QC of bulk drug substance and drug product in a multi-product facility. Perform duties under limited supervision and according to standard operating QC procedures. Execute independently with adequate training fundamental operations such as HPLC and Capillary electrophoresis. Perform 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. Adhere to established regulations and follow cGMP established by site. Report abnormalities and deviations in a timely and accurate manner. Adhere to safety standards and identifies unsafe situations/ habits and escalates appropriately. Maintains work production areas according to predefined standard (5s). Experience: Bachelor's Degree in Life Sciences required. Level II: 5+ years of relavent industry experience. Level III: 8+ years of relavent industry experience. GMP experience is highly preferred. Demonstrate strong interpersonal and communication skills (both written and oral). Demonstrates ability to work independently and as part of a team, to meet departmental/facility goals. Fladger Associates