Avishek Ganguly

AVISHEK GANGULY Experienced and reliable Quality Control professional with over four years of experience working in companies to ensure the highest quality outcomes possible. WORK EXPERIENCE LUPIN LTD, Bhopal (API & Formulation-USFDA, MHRA, TGA) Officer (QC-GLP) CONTACT PHONE NUMBER: - EMAIL ADDRESS:-ADDRESS: Old Calcutta Road, Patulia Kolkata- 700119 March 2021-Present • Responsible for performing calibration of Instruments and Equipment's as per schedule. • Qualification and maintaining of various standards used for analysis and calibrations. • Instruments handled like HPLC (Agilent, Shimadzu), pH, UV (Shimadzu), FTIR (Shimadzu), TOC (Shimadzu), KF (Metrohm), Polarimeter (Rudolph), Melting Point (Buchi), Conductivity meter, Analytical balance (Mettler Toledo, Sartorius), Sieve Shaker, Tap Density and Bulk Density Apparatus. • Responsible for preparation of annual schedule, and documentation for change control and other non-conformance. EDUCATION BACHELOR OF PHARMACY CGPA (7.7/10) Maulana Abdul Azad University of Technology August 2015-July 2015 SKILLS • • • Strong Communication Disciplined Fast Learner MICRO LABS LTD, Sikkim- (Formulation) Senior Executive (QC-GLP) November 2019-Jan 2020 • Responsible for performing daily calibration of Instruments and Equipment as per schedule. • Instruments handled like HPLC (Agilent, Shimadzu), UV(Shimadzu), FTIR (Shimadzu), TOC (Shimadzu), Polarimeter (Rudolph), pH, Conductivity meter, Analytical balance (Mettler Toledo, Sartorius). • Reporting and documentation of IOP, EOP with change control. LANGUAGE • • • English Hindi Bengali ACHEIVEMENTS • • • • • • NCC A-Certificate (Flying Division) Six Sigma White Belt (SSCD) Computer Skills (NIIT) Internship in CRI Institute, Kasauli (GOI) Internship in Dey's Medical, Kolkata Certification of Drug Registration and Listing (USFDA) HOBBIES • • • Photography Music Reading CIPLA LTD, Sikkim- (Formulation) Senior Executive (QC-RM) December 2015-October 2019 • Responsible for performing analysis of pharmaceutical Raw material (API and Excipient), Water, Compressed air and Nitrogen gas as per guidelines with simplification and accuracy. • Creating Test data sheet and other forms of documentation and reporting in LIMS and SAP as per SOP's/ Guidelines. • Identification of contaminants, including residues in pharmaceutical raw materials. • Keeping updated guidelines and SOP's for the current working effectiveness with imparting the training to other peers. ZYDUS HEALTHCARE Production Officer (Operations) July 2015-December 2015 • Operating and Testing in-process product like Tablet, Capsules and work between shifts and documentation. • Observed production work and made corrective performance. • Managing and maintaining daily records with any dues. • Productive outputs with zero errors and Non Conformance