Executive - Quality Control

You will be responsible for analyzing raw materials, in-process, and finished product stability samples of various formulation products such as oral solids and injectable ophthalmic products. This includes utilizing QC Instruments like HPLC, GC, UV, FTIR, pH Meter, etc. You should have exposure to software like Empowers and Labware LIMS and possess knowledge of GLP GDP practices. Your role will involve executing validation, qualification, and calibration activities in the QC laboratory, as well as preparing SOPs, GTPs, STPs, specifications, protocols, IOCPs, records of analysis, and analysis reports. You will also be responsible for handling, issuing, and maintaining consumables, glassware, chemicals, reference standards, working standards, and cinematographic columns. Candidates with exposure to regulatory audits like USFDA will be preferred. Additionally, you will be required to review various types of samples and documents, including raw materials, finished products, stability samples, qualification documents, and calibration AMT documents. Your responsibilities will also include investigating OOS test results and laboratory incidents, as well as ensuring compliance with safety standards and maintaining Good Laboratory Practices at all times.,