Executive - Quality Control

Job Description:

• To execute analysis of finished goods / Stability samples / Raw materials / Packing materials In-process and cleaning samples along with relevant laboratory documentation.
• Intimation & result reporting after completion of analysis & relevant documentation.
• Before starting an analysis, following points (but not limited to) must be checked:
• Check all the instruments on the equipment required for the analysis are in working condition and are in calibrated state.
• Checking and ensuring proper status labels after confirming availability of all the requirements (as applicable) for analysis such as approved control procedure, analytical protocol, reference standards, chemicals, reagents, GC/HPLC Columns, glassware, water preparation equipment, water bath, sonication baths, mobile phase bottle etc.
• Ensure the online documents pertaining to day-to-day analysis are efficiently completed in timely manner. Reporting the activities daily to immediate supervisor.
• Ensure timely calibration & preventive maintenance of equipment/instrument.
• Destruction of respective records & QC samples like retention samples of raw materials, analyzed samples.
• To take out the quality reports, data / results entry in SAP system.
• To prepare and maintain the working standards & documentation.
• Ensure timely raising and closure of deviations, quality events, change controls, OOS/OOT.
• Execution of analytical method validation, cleaning validation of products.
• Preparation and maintenance of Analytical data sheets and Excel spread sheets.
• Adequate knowledge of all equipment/instruments & their functioning in the laboratory & assist in equipment/instrument qualification activities.
• Ensuring the quality and integrity of all GxP data and documentation generated.
• Ensuring effective execution requirements of food regulations (US)-21 CFR Part 111.
• Ensure fully Engagement and Involvement regarding awareness, clarity maintained related to data integrity.
• Ensure the 21 CFR Part 11 compliance in the laboratory.
• Effective implementation of practices like cGMP & GLP, ISO 9001, ISO 14001, ISO 22000,  ISO 18001, HACCP and SQF in QC Dept.
• To follow and maintain the standard chromatographic practices.
• Ensuring good house-keeping and accident free working in the laboratory.
• To perform safe Laboratory operations (as per MSDS) ensuring proper usage of PPEs, safe, secure storage of hazardous, toxic, explosive, corrosive, irritant materials.
• Ensure proper maintenance of HPLC and GC column and related logbooks in QC lab.
• To fulfill the analytical requirements of FSSAI regulation.
• To undergo assigned trainings on cGMP, HSE & departmental procedures / policies. 
• To determine internal and external QEHS issues as well as needs and expectations of relevant interested parties and monitor the same.
• To implement QEHS policy & objectives.
• To ensure participation and consultation of worker.
• To identify & communicate incidents, QEHS non conformities, investigate and take corrective actions on the same.
• To ensure work permit system during maintenance activities.
• To implement QEHS continual improvement projects at site and monitor.