Synbiotics Limited

Role & responsibilities Sampling and analysis of Raw Materials, In-process samples, Finished Products , and Stability samples as per SOP and test methods. Preparation and standardization of volumetric solutions, reagents , and reference standards . Performing routine chemical, instrumental (HPLC, GC, UV, FTIR), and microbiological testing (for applicable roles). Equipment/instrument calibration and maintenance logs. Participation in method validation , stability studies, and process validation activities. Adherence to Good Laboratory Practices (GLP) and regulatory standards. Supporting internal and external regulatory audits (like USFDA, WHO-GMP). Reporting deviations, OOS results, and non-conformities. Carrying out any other responsibilities assigned by the QC Manager/Head. Preferred candidate profile Educational Background: B.Sc. or M.Sc. in Chemistry Experience Range: 1 to 6 years in Quality Control (pharma API, fermentation, or biotech industry preferred). Technical Proficiency: Hands-on with analytical instruments such as HPLC, GC, UV, FTIR, pH meter, and KF Titrator . Familiar with wet chemistry techniques and reagent preparation. Documentation & Compliance: Well-versed with GLP, GMP, and cGMP practices. Ability to handle SOPs, test methods, logbooks , and regulatory documentation. Behavioral Traits: Detail-oriented, punctual, and safety-conscious. Willing to work in shift duties and perform repetitive precision work. Good communication skills and the ability to work in a team under supervision. Location Preference: Candidates from Vadodara or willing to relocate will be preferred.