Biodata |
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| Name of the Candidate | : | [Private] |
| Name of the Post Applied | : | Quality Assurance Executive |
| Job related skills / software | : | Preparation and Review of standard operating procedures (SOP’s), Preparation & review of the Annual Product Quality Review reports, Handling of Change control & Deviation control. |
| Category | : | Medical |
| Sub Category | : | Quality Assurance Executive |
| Years of Experience | : | 10 years |
| State | : | Telangana |
| Gender | : | Female |
| Salary Expected per Month(Rs) | : | 50,000 to 60,000 |
| Highest Qualification attained | : | M.Sc. / MSC : Master of Science |
| Major / Specialization | : | Chemistry |
| Email Id | : | [Private] |
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| Are you looking for job now? | : | Yes |
| Can the recruiter contact you? | : | Yes |
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Resume Format / CV Sample Template / Example / Model : |
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T.MANJULA
E-MAIL : mallimanju21 AT gmail.com
CAREER OBJECTIVE :
Seeking a challenging position in Quality Assurance Department for a suitable position where utilizes my skills and technical abilities in the pharmaceutical field that offers security and professional growth while being resourceful, innovative and flexible.
EXPERIENCE :
Working as Executive– QA at Hy-Gro Chemicals Pharmtek Pvt. Ltd.IDA Bollaram, Sangareddy Dist, Since October 2010 to till date.
STRENGTHS :
** Ability to work as a team member to meet customer / organizational needs.
** Fast and dedicated learner.
** Commitment, dedication towards job until completion.
** Performance to meet the ICH requirements
EDUCATIONAL PROFILE :
** M.Sc. Chemistry from Kuvempu University.
** B.Sc (Microbiology, Botany, Chemistry) from S.V University
COMPUTER LITERACY :
Packages :
MS – Office, Chem Draw & ACD Chem Sketch
Operating system :
Windows –98, 2000, XP & Millennium
Typing :
Lower in English
JOB RESPONSIBILITIES
Quality Assurance Activities :
** Preparation and Review of standard operating procedures (SOP’s)
** Preparation & review of the Annual Product Quality Review reports.
** Handling of Change control & Deviation control.
** Handling of Out of Specifications
** Handling of customer complaints
** Review of calibration records of all QC instruments
** Giving Response to customer Questionnaires.
** Review & approval of final product quality data and certificate of Analysis.
** Preparation and Review of Process validation, Method validations and Cleaning validation protocols & reports.
** Preparation of Site Master File (SMF) & Validation Master File (VMP) as per guidelines.
** Review of Stability & Hold time study protocols & Reports.
** Review of Master Formula and Technical Packages.
** Review of Batch Manufacturing Records (BMRs) & its Raw data sheets for the manufacture of API’s, Intermediates.
** Conducting Internal Audits for all the departments as per ISO & ICH guidelinesand ensure
** Daily Plant inspection for the implementation of GMPs.
** Well versed in preparation of all types of documentation work related to all departments.
** Performing vendor Assessment program (Vendor rating & Annual evaluation).
** Responsible for Supporting Documentation work related to Internal Audits, Customer Audits and Regulatory requirements.
** Daily Monitoring of plant observations & Review of Calibration Reports (Internal &External)
** Handling dispatches of Formulations.
PERSONAL PROFILE
Husband Name : T.
Mallaiah
Date of Birth : 19 / 01 / 1989
Marital Status : MARRIED
Languages Known : ENGLISH, TELUGU & HINDI.
DATE :
PLACE :
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