Nayna Patel Email Address

Senior Quality Control Stability Supervisor

Since 1919, G & W Laboratories has developed, manufactured, and marketed pharmaceuticals designed to alleviate human suffering. We serve our customers by providing quality pharmaceuticals, valuable services, and timely information while remaining responsive to an ever-changing marketplace. We accomplish these objectives by building upon our unique history, while anticipating the future needs of the marketplace and responding quickly. These are the enduring principles guiding our organization: We shall conduct ourselves with integrity and honesty. We shall treat our employees, customers, vendors, competitors, regulatory agencies, the community and the environment with respect and fairness. We shall strive to build a profitable organization of highly motivated employees committed to working together to achieve company goals and individual professional and personal growth. We shall adhere to the laws of the land and uncompromising ethical standards as we pursue our business objectives. Lastly, and with humility and gratitude to all who contribute towards our success, we shall not forget those in need and shall continue to contribute a significant portion of our profits to charity. gutter Consumer Products | Contract Manufacturing | International Sales | Healthcare Professional Info | Career Opportunities Home | Contact Us | Site Map | FAQs Comments to: webstaff@gwlabs.com | Corporate Phone Number: 800-922-1038 Legal Notices| Privacy Policy

-Managed the stability program as per cGMP and under compliance that include the following tasksoPlacing the product into appropriate stability chamber and withdrawing stability sample as per stability protocoloScheduling testing, reviewing data, entering and trending data into ScienTek software.oPreparing APR report for all the marketed product to support current expiration date of the productoSubmitting stability data for annual filing for ANDA productsoSupported Finish product release, customer complaint, and deviation during manufacturing with stability data, and extending expiration dateoIn case of confirmed stability failure warranted recall of the product from the marketoMaintained all stability chambers in compliance-Created and edited SOPs, Chemical Testing Monographs for finished products and raw materials, specification and analysis reports for finished product, stability and raw material.-Generate stability protocols for G&W drug products -Effectively managed all QC activities that include scheduling work to the chemists, reviewing data for FDA and cGMP compliance, releasing raw materials, in-process, finished products, stability samples, process validation and complaint samples. -Provided training on lab procedures-Conducted performance evaluation on yearly basis -Prepared OOS and OOT reports -Interacted with outside labs and vendors for storage and/or testing of stability samples and resolve issues related to OOS.-Created Residual Solvent Statements for G & W drug products as per USP/FDA requirements. -Reviewed IQ/OQ/PQ protocols and SOPs generated by the Metrologist -Developed, documented and implemented programs for in-house standard verification and Vendor qualification of raw materials.-Actively interacted with FDA outside Auditors during FDA inspections and audit-Interacted with other department such as QA, ARMD, TS, and RA to provide various informationSpecialties: -Maintained Empower program used in the lab to collect chromatographic dataoCreated custom project (about 200) for finished products, raw materials and equipment calibration oEach project is product specific and is created to generate reports with the final results (automatic calculations) and audit trail information. oCreated new versions and Archive ProjectsoTrain chemists in the operation of the Empower software and troubleshooting problems related to Empower operation