Nageswararao

Working as a QC Manager. Looking for job any where
39 years oldOther technical positionsCome from India Living in Tianjin
Language: English, Hindi
RESUME --------------------------------------------------------------------------------------------------------------------- NAGESWARA RAO MUNAGA Mobile no: +8613439223395:+8613261199250 E-mail: nmunaga@yahoo.com --------------------------------------------------------------------------------------------------------------------- CAREER OBJECTIVE: To make a challenging career by working in an esteemed organization where i can implement my experience and prove my technical skills to the fullest of my extent. If I am selected for the post, I can assure you that I will do my best and dedicated service to your organization. PROFESSIONAL EXPERIENCE: TOTAL EXPERIENCE: 10 years 3Months. 2018 0ctober - Present. Asym chem, China. Position: QC Manager. Reporting: Director. Responsibilities:  Analytical method validation, verification, cleaning validation, stress study of product and method transfer protocols and reports review.  Participate in Investigations for OOS, OOT and Deviations and execute CAPA.  Chromatographic data Processing review as per GCP.  Good exposure in chromatographic review, data review.  Training conduct for new joiners.  Organize team to carry out continuous optimization to improve compliance and work efficiency.  Strong communication and organization coordination ability, good planning management, data analysis, presentation and reporting capability.  Involved in Internal, Customer and external regulatory audits like USFDA and CFDA.  Monitoring lab functions as per CGMP. 2016 April – 2018 0ctober. Beijing Sciecure Pharmaceutical Co., Ltd China. Position:Analytical chemist. Report: Manager and Director. Responsibilities:  Analytical method validation, verification and method transfer for validated methods.  Participate in Investigations for OOS, OOT and Deviations and execute CAPA.  Sample analysis, data Processing and documentation as per GMP.  Good exposure in chromatographic analysis, data review, instruments calibrations, wet analysis and trouble shooting.  Cleaning validation, stress study of product as per protocol.  Involved in Internal, and external audits like Customer, USFDA, MHRA, TGA and WHO audits.  Lab instruments Calibration log books review.  Preparation of Analytical method validation, working standard protocols and reporting.  Online record updating, working based on CGMP.  To carry out the calibration of Instruments, maintaining log records.  Good exposure in chromatography, analysis, data review, instruments calibrations and trouble shooting.  Analysis data review of formulated products, and API materials with respect to specifications and customer requirements (instrumental & chemical). 2015 Sep – 2016 Feb. Micro labs limited Bangalore. Position:Senior Executive. Report:Manager and Director. Responsibilities:  To carry out the calibration of instruments, maintaining log records.  Preparation of certificate of analysis. Follow up Calibration of Instruments as per the scheduling dates.  Good exposure in chromatography, analysis data review, instruments calibration trouble shooting.  Wet analysis data review of formulated products, APIs and its intermediates and Raw materials.  Dissolution testing of formulated products like capsules and tablets by HPLC or UV data review.  Online record maintenance and working based on CGLP. Work allocation and leading a team as per shift schedule.  Participate in Investigations for OOS, OOT and Deviations and execute CAPA.  Analysis electronic data review and documentation review.  Involved in Internal, and external audits like Customer, USFDA, MHRA TGA and WHO audits.  Lab instruments Calibration data review. 2013 Sep – 2015 Sep. Cipla ltd, Bangalore. Position:Management staff. Report: Section head. Responsibilities:  Participate in Investigations for OOS, OOT and Deviations and execute CAPA.  Analysis of electronic data Processing and submission (21CFR part 11).  Involved in Internal, and external audits like Customer, USFDA, MHRA TGA and WHO audits.  Work allocation and leading a team as per shift schedule.  Lab instruments Calibration data review.  Lab functions maintaining through Quality management system (QMS).  Stability samples analysis of data review.  Online record updating (Online documentation), working based on CGLP.  To carry out the calibration of instruments, maintaining log records  Good exposure in chromatography, analysis, data review, instruments calibrations and trouble shooting. 2010 Oct – 2013 July. A.F.T. Pvt. Ltd, Hyderabad. Position:Senior Chemist. Report:Manager. Responsibilities:  Analytical method validation, verification and method transfer for validated methods.  Participate in and lead Investigations for OOS, OOT and Deviations. Participate and execute CAPA.  Sample analysis, data Processing and documentation as per GLP.  Good exposure in chromatographic analysis (HPLC and GC), data review, instruments calibrations, wet analysis and trouble shooting.  Work allocation and leading a team as per shift schedule.  Cleaning validation, stress study of product as per protocol.  Determination of solution stability of product. 2005 Aug – 2007 Sep. ALPHINE PHARMACEUTICALS Ltd, Hyderabad. Position:Chemist. Report:Manager. Responsibilities:  Preparation of certificate of analysis. Follow up Calibration of Instruments as per the scheduling dates.  In process analysis both wet analysis and instrumentation analysis.  Good exposure in chromatography, analysis, instruments calibrations and trouble shooting.  Wet analysis data review of formulated products, APIs and its intermediates and Raw materials.  Preparation of volumetric solutions and standardization.  Maintenance of in process Records & documentation.  Good exposure in chromatographic analysis (HPLC and GC), instruments calibrations, wet analysis and trouble shooting.  Lab instruments Calibration data review.  Online record updating, working based on GLP  To carry out the calibration of equipments, instruments and maintaining log books.  In process samples, API and formulated products like capsules and tablets analysis. TECHNICAL EXPERTISE: • HPLC, GC, Polari meter, • UV- visible spectrophotometer, • Disintegration apparatus, • Dissolution apparatus. INSTRUMENTS HANDLING:  HPLC-Waters (Empower Software), Shimadzu (LC Solutions Software) Agilent technologies(Open lab and Chromeline Software),  GC-Shimadzu (GC Solutions), Chemito GC-1000(IRIS-32),  UV-Visible spectrophotometer-Shimadzu,  Dissolution-Vision classic,  Disintegration test apparatus-Electro lab,  Friability –Erweka,  PH meter- Polmon,  MR meter –Polmon,  Analytical balance- Mettler Toledo,  KF Titrator- Polmon,  Polari meter-Advance,  TDS/Conductivity analyzer-Polmon,  UV Chamber-Vision. EDUCATIONAL QUALIFICATIONS:  2010 M.Sc Analytical Chemistry from S.V.University, Thirupathi, A.P.  2005 B.Sc (BZC) from Acharya Nagarjuna University, Guntur, A.P.  2002 Intermediate (Bi.P.C) from Govt Jr college Gurazala, A.P.  2000 SSC Fatima high school Dachepalli, A.P. PERSONAL DETAILS: • Father’s name: Ramulu, • Date of birth: 09/08/1985, • Sex: Male, • Marital Status: Married. • Nationality: Indian, • Languages known: Telugu, English, and Hindi, • Address for communication: H.No:5-32A, Chapala bazaar, Dachepalli (villa & Mandal), Guntur (Dist), A.P, 522414. DECLARATION: I hereby declare that the above mentioned information is true to my knowledge and I bear responsibility for the correctness of the above mentioned particulars. Place: Date: (NAGESWARA RAO MUNAGA)