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[QUOTE=Guest-IJT;93798][b][u]CURRICULUM VITAE [/u][/b]: RAGHUVEER. [b][u]JOB OBJECTIVE [/u][/b]: - Career development and growth through employment with the company.. - Application of skills through result oriented and innovative working. - Continuous personal development through new skills building and learning. - To grow up as a more matured human being and a responsible citizen. - To find a stable and challenging long-term position that will allow me to increase my standing within the engineering and standards communities. [b][u]KEY ROLES -RESPONSIBILITIES [/u][/b]: - Having Good Knowledge & Work Experience for Analytical method validations. - Technical co-ordination for Quality assurance to be inline with regulatory requirements. - Responsible to Ensure the Systems, facilities, Procedures are in Adequate. - Responsible to ensure Quality operations are clearly specified and maintenance of GMP. - Internal Auditor for plant self inspection, Quality Audit. - cGmp & Glp trainer to the trainees at work place. - Supervise control activities like OOS, failure investigation. - Responsible for change controls, document control, and deviation control, and control of non-conforming products. - Possess excellent interpersonal, analytical, troubleshooting and team building skills with proven ability in establishing quality systems. [b][u]WORKING PLATFORM [/u][/b]: - Control of In-process activities and validations execution. - Review of Quality control, Quality Assurance, Engineering, warehouse and production standard operating procedures. - Well acquainted with latest Regulations for Complete Process Monitoring methods, cGMP Guidelines. - Review & approval of raw data of analysis, protocols, STPs, COAs as per GMP practices. - Review and approval of method validation data, stability protocols, and sampling protocols. - Review & approval of Trend analysis, Annual Product Report - Review of raw materials and finished products. - Review and approval of compilation data for stability studies. - To monitor Control samples of Finished Products and scheduling of Accelerated and long-term Stability Studies. - Keen role in handling and educating trainees and subordinates. - To ensure and control Good laboratory practices in QC laboratory. - To ensure the Installation, Operational and Performance Qualifications of Equipment related to laboratory (HPLC, GC, FT-IR and etc.). - Well versed in Handling Equipment’s like HPLC, GC, UV-VIS, IR, KF-Auto titrator, Tapped density, potentiometer and Particle size analysis etc… - Looking after General Administration of Laboratory, indenting of various Chemicals, Reagents, Equipment spares, and other lab consumables - Maintaining Scheduling dates for various Equipment Calibrations and documenting supporting documents and recording of various documents related to GMP and GLP. - Well versed in Handling Equipment’s like HPLC, UV-VIS, IR, Dissolution apparatus, KF-Auto titrator, & etc. - Calibration of all Instruments, & Glassware’s. - Product Rejection, Process fault Analysis, & Route Cause Analysis.. [b][u]PROFESSIONAL EXPERIENCE [/u][/b]: [b][u]1) Organization [/u][/b]: Dymes pharmachem Limited. [b][u]Designation [/u][/b]: Quality Manager. [b][u]Department [/u][/b]: Quality Control & Quality Assurance [b][u]Duration [/u][/b]: Jan-2007 to till date [b][u]Location [/u][/b]: Hyderabad, Andhra Pradesh. [b][u]2) Organization [/u][/b]: Symed Labs Limited. [b][u]Designation [/u][/b]: Quality Control Manager. [b][u]Department [/u][/b]: Quality Control. [b][u]Duration [/u][/b]: May-2005 to Jan-2007 [b][u]Location [/u][/b]: Hyderabad, Andhra Pradesh. [b][u]3) Organization [/u][/b]: Sipra Labs Limited. [b][u]Designation [/u][/b]: Group Leader (Approved chemist) [b][u]Department [/u][/b]: Quality Control. [b][u]Duration [/u][/b]: Sep-1994 to May 2005. [b][u]Location [/u][/b]: Hyderabad, Andhra Pradesh. [b][u]4) Organization [/u][/b]: Sreepathi Pharmaceuticals Limited. [b][u]Designation [/u][/b]: Chemist. [b][u]Department [/u][/b]: Quality control. [b][u]Duration [/u][/b]: 1993 to 1994 [b][u]Location [/u][/b]: Hyderabad, Andhra Pradesh. [b][u]5) Organization [/u][/b]: Shilpa Antibiotics Private Limited. [b][u]Designation [/u][/b]: Chemist. [b][u]Department [/u][/b]: Quality control. [b][u]Duration [/u][/b]: 1991 to 1993 [b][u]Location [/u][/b]: Raichur, Karnataka. [b][u]EDUCATION [/u][/b]: - Master of Science in Chemistry from Nagarjuna University – Guntur. (A.P) - Bachelors in Science from Gulbarga University – Gulbarga. (Karnataka state) [b][u]STRENGTHS [/u][/b]: - Positive Attitude. - Good grasping and analytical ability. - Self-motivation. - Result oriented working. - Keen observation. [b][u]Date [/u][/b]:[/QUOTE]
