plastemartjobs.com Email: jobs@plastemart.com, hr@plastemart.com Download Date: 6/1/2025 7:01:12 PM ________________________________________________________________________________________ RefNo: CA - 17544 Gender: Male Age: 49 Designation: Sr.Executive Quality Control Highest Education Level: Masters - Degree Education Details: M.Sc.(Chemistry) from Vinayaka Mission University, Skill Sets: AREA OF INTEREST Production, manufacturing, Quality, R&D and packaging. Work Experience: 18.3 Work Experience Details: Sr.Executive Quality Control Since October 2018 to July 2020. Company profile- Manufacturer of Nutracuticals,cosmetic,personal care,home care products and ayurvedic medicines Sr.executive Quality Assurance & Control From July2016 To June 2017. Company profile- The National Medicinal Plants Board Executive QA/QC Since Apr 2010 to Jan 2016. Emami Ltd.,Pantnagar Company Profile: Manufacturer of Pharma, Ayurvedic, cosmetics & FMCG products? Job Profile: Ensure analysis of all samples of incoming herbs, milk, raw materials(chemicals), edible oils as rice bran oil, til oil, almond oil, olive oil (including ?iodine value, peroxide value, sap value, acid value, free fatty acid, unsaponifiable matter and total fatty matter), packing materials, semi finished product and finished product in time. Preparation of QA/QC reports and interaction with stores and production departments. Strictly adherence of R&D specifications, test procedures and CQA guidelines. Internal and external calibration of testing equipments. To monitor documents related to external lab testing and external instrument calibrations. Ensure all suppliers used by organization are R&D approved and maintain record of this. Ensure QMS in daily working and minimization of gaps observed in internal and external audits for continual improvements and QMS conformance. To arrange necessary training and assessments of all laboratory personnel. To guide analysts in review of current procedures in laboratory. To ensure compliance with mandatory regulatory requirements like FDA, ISO etc. Investigation of customer complaints and implement corrective and preventive actions. To ensure corrective and preventive actions are recorded and reviewed. Evaluation of analytical trends of routine samples, control samples and market samples for continual improvement process. To control storage and handling of analytical data and control samples and destruction of the same as per SOP for control of quality records. Ensure all laboratory operations in accordance with GLP. Ensure compliance of GMP. Online quality control monitoring and finished goods AQL testing. Implementation of SOPs and CQA guidelines. To communicate out of trend, out of specification results, online issues encountered during material use and rejections to suppliers for trouble shooting in-house if possible or to follow up for lifting or destruction of rejected materials if any in stores. To check and approve complete BMR/BPR. Verification and monitoring of QC released materials as per FIFO/FEFO system. Verification and monitoring of exact quantities of materials specified in BMR/BPR, product wise and batch wise dispensing of ingredients. To monitor and ensure critical steps during manufacturing, filling and packing process and countersign the same in BPR. To ensure withdrawal of appropriate analytical and control samples of each and every batch and maintenance of record of the same. Daily water system monitoring and verification of QCPs by lab testing. Monitoring and tracking of CIP activity of plant manufacturing and filling machines as per CQA guideline. Maintenance of statutory norms like PCRO Authorities: Release and rejection of raw materials. Lab reagents, glassware and equipment's procurement. Clearance of bills of external testing, external calibrations or repairing services/AMCs of lab instruments and external pest control service agencies. Editing results, task list creation and increase shelf life expiry date of raw materials after retesting in SAP system. Preparation of COAs for finished goods exported. Preparation FDA applications for new products. Procurement of necessary documents as R&D ?TTDs, R&D specifications of new RMs, test procedures, lab reagents, glassware and equipments required for RM testing, semi finished product, finished product manufacturing of new products/ formula change as well as trial/commercial batch manufactured by R&D. Instruments Handled: G.C. (Nucon 5765, Eshika) H.P.L.C (Waters 2695, 515 separation module equipped with millennium 32, Empower 2 software). UV Spectrophotometer (Perkin Elmer-Lambda EZ 201, Shimadzu-1800) Polarimeter (Perkin Elmer- 341) Karl Fischer Titrator (EI-761 E) Melting Range apparatus (Scientific ? MP-DS) pH Meter ( ESICO-1012 E) Conductivity Meter (ESICO-1601) Penetrometer Refractometer Viscometer (Brookfield LV & RV) Asstt. Executive Q.C Sep 2007 to Mar 2010 Company Name: Mayuka Labs Pvt. Ltd. Company Profile:Manufacturer of Montelukast intermediates & API Quality Checker Chemist May 2005 to Aug 2007 Company Name: Morepen Laboratories Ltd. Company Profile: Manufacturer of intermediates and APIs of Bulk drugs like Loratadine, Fexofenadine, Atorvastatin calcium, Sultamycillin and Montelukast sodium ________________________________________________________________________________________