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CV for Sep, 2015 updated


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CV for Sep, 2015 updated

  1. 1. CURRICULUM VITAE PVRSN Reddy. Email: SR Estates, 7th Block, Flat No. G4, Miyapur, Hyderabad. Mobile: 8096934635 CAREEROBJECTIVE Having 11 years experience in Quality Control and Laboratory functions in Drugs and Pharmaceutical Industries (Formulation) in different organizations in different positions. ACADEMIC QUALIFICATION  BSc., (Andhra University)  MSc., (MKU)  Computer skills in MS Office and Type writing. CAREERHISTORY  Talwar Pharma. Roorkee, Uttarakhund. (May’ 2013 –Apr’2015) (Tablets, Capsules and Pellets) Position: Quality Control Incharge.  Primus Pharmaceuticals, Kala Amb, Himachal Pradesh (May’ 2010 –Apr’ 2013) (Tablets, Capsules and Pellets) Position: Quality Control Incharge.  Talwar Pharma, Roorkee, Uttarakhund. (Aug’ 2007 –Apr’ 2010) (Tablets, Capsules and Pellets) Position: Quality Control Incharge  BL Pharma Limited, Hyderabad. (Oct’ 2003 –Jul’ 2007) (Tablets, Capsules and Syrups) Position: Approved Analytical Chemist.
  2. 2. PROFESSIONAL SKILLS (Instrumentation and Chemical)  Raw material, Packaging material, In process and Finished productanalysis.  Analysis of Pellets, Tablets, Capsules, Syrups, Ointments, Creams, Lotions, Powders, Sustained releaseproducts.  Preparation of working standards.  Preparation of volumetric solutions and their standardization and preparation of reagents, buffer solutions and indicators.  Handling of HPLC, FTIR, UV and other equipments in the laboratory.  Preparing SOP’s, STP’s, BMR’s, BPR’s for raw material, packaging material, in process and finished productand general SOP’s.  Control of SOP’s and other documents in the laboratory.  Prepare and maintain Log books, Total preventive maintenance and Calibration for all equipments.  Knowledge about Method validation, Equipment validation and Cleaning validation.  Handling of stability study analysis for long term and acclerated.  Knowledgeabout IP, USP, BP and other procedures/requirements.  Conducting of self audits in the laboratory to improvequality system.  Technical and Analytical skills to improveproduct quality.  Approving/Rejecting of Packaging material, Raw material, In process and Finished product analysis.  Good coordination with other departments.  Handling of all activities in the laboratory.  Knowledge about Quality Assurance department activities regarding preparation and control of SOP’s and documents, monitoring all activities in different stages in production.  Good knowledgeof MS office.  Having knowledge in Quality Control, Quality Assurance and Production to improvequality. APPROVAL IN QUALITY CONTROL DEPARTMENT Having approvalin Chemical and Instrumentation analysis as approved by The Directorateof Drugs ControlAdministration, Governmentof Andhra Pradesh from 2003.
  3. 3. AREAS OF EXPERIENCE QUALITY CONTROL  Analsysis.  Preparation of formats and other related documents.  Documentation.  Different activities in the laboratory. QUALITY ASSURANCE  Preparation of documents.  Control of Documents.  Different activities in Laboratory and Production. PRODUCTION  Manufacturing process of Tablets.  Manufacturing process of Capsules.  Manufacturing process of Pellets.  Documentation. PERMANENTADDRESS PVRSN Reddy, Eleatipadu, Iragav aram Mandal, West Godavari District, AP. PERSONAL INFORMATION o Languageskills: Telugu, English and Hindi. o Hobbies: Reading, Playing and Tourism. o Married. Yours faithfully, PVRSN Reddy.