Role and Responsibilities: Support for reagent and solvent management Support for Glassware management Support for reference standard management Support for Column management Support for record management Support activities like general lab inventory management etc. Support for Instrument inventory management Support for calibration of analytical accessories management Support in shipment management related activities eg: shipment of reference standards, samples etc. Receipt of material and GRN completion of purchase request(s) in applicable system on site. Responsible to support Life cycle management activities of instruments and equipments Responsible for handling data related to laboratory support activities as per the applicable lab procedure. Like CIMS data for reagent solvent management, COA for Column management etc. Minimum Qualification for the position: Science/Pharmacy Graduate and Adequate computer proficiency. Adequate knowledge of verbal and written communication skills in English Must be able to work independently with minimum supervision to meet deadlines and maintain a positive attitude. Minimum 2 years relevant experience.

Role Overview Responsible for review of qualification & calibration data of instruments and equipment as per procedures with QMS. Illustrative Responsibilities Ensure that qualification & calibration activities are planned and executed within time frame defined by the procedure and equipments are released on time as per the pre-defined schedule. Responsible for coordinating with lab supervisors / system owners for handling of any non-conformances or escalations Handling of QMS related activities like, Change control, CAPA and Deviation with its effectiveness check. Responsible for quality compliance activities for laboratory instruments qualification and calibration. Summarize, review, and report the analytical Instruments qualification and calibration for further approval. Ensure a disciplined work environment to provide expertise to subordinates colleagues in the proper performance of laboratory procedures. Ensure on time GDP in technical function with right first time (RFT) approach. Responsible for ensuring team compliance to EHS, Quality & Business policies Any other work given by management from time to time. Quality & Compliance Responsible for following GMP/GLP/ GDP/EHS policies by self as well as the team Required skills Technical expertise in Analytical instruments qualification, calibration, protocol preparation and QMS. Build cohesive team valuing team spirit Able to anticipate the implications and consequences of situations and take appropriate actions in the interest of Client as well as Cal Scientific without compromising quality. Clear thoughts and effective and crisp communication. Job requirement M.Sc – specializing in Chemistry/ M. Pharma with proven experience of min. 7-8 yrs. in Instrument qualification and calibration. In depth experience in Chromatography (HPLC, UPLC, GC), Spectroscopy (MS, FTIR, UV), Thermal techniques (DSC, TGA) and Particle size measurements. Expertise in analytical instruments qualification and calibration, protocol preparation, CAPA, Investigations, Deviations (QMS) Good Knowledge of ICH guidelines and different global regulatory authorities.

JD: Inventory Management FTE The employee is responsible for performing activities in compliance with current established procedures of Safety and Quality. Main and additional duties are mentioned below: Responsible for Inventory management for Lab chemicals/Solvent, Reference standard including procurement, receipt, issuance. Responsible for Inventory management for Glasswares, including procurement. Responsible for Inventory management for Lab stationary items, including procurement, receipt, distribution. Responsible for executing activities in EDMS as per assigned roles and as per applicable procedures. Responsible for Inventory management for chromatography columns, including Procurement. Responsible for creation of GRN for Lab related items. Responsible for maintaining various databases in the lab. To execute the task according to the cGMP guidelines. Responsible for filing of ELIMS worksheets and other documents. Responsible for all the activities assigned in the Lab responsibility list. knowledge of excel/ pivot table. Ability to extract technical information, such as given on SDS, COA, test method for a specified reagent and then place the order GMP Responsibility •To execute the tasks according to the cGMP guidelines and established laboratory procedures. •To document execution details contemporaneously and verify completeness of execution record as per established laboratory procedure. •To always comply with procedure and ensure lab is in state of audit readiness. Quality & Compliance Responsibilities •To ensure that respective guidelines on data integrity and laboratory control processes are followed as per established SOPs. •To ensure immediate escalation of issues/observations not in conformity with applicable procedures /policies etc.