Looking for an opportunity in prestigious organization where I am exposing to my experience and abilities in Pharma field besides improving my skills and learning new technologies.Educational Qualifications :
M.Sc chemistry from Bharthidasan university with 63% of marks in May 2007,at Tirchy
B.Sc. (M.P.C.) from Andhra University with 63% of marks in April 2004, at Chintalapudi
Intermediate from Chaitanya Bharathi Junior College with 59% of marks, in March 2000,at Chintalapudi.
Board of Secondary Education from Santhinikatan School with 59% of marks,in March 1998 at Raghavapuram.Technical Skills :
Internet surfing and mailingStrengths :
Honest and Dependable with Excellent Interpersonal skills.
Team oriented Organized and Manage Time well.
Work well under pressure, Flexible and Quick learner.
Possess Leadership skills; Enthusiastic and Assertive.Present Experience :
Having Post Graduation in chemistry and around 3 plus years experience in various pharmaceutical industries. Presently working in Pravah Laboratories Pvt Ltd., as a Executive in Quality Assurance at location of Yadagirigutta (mandal), Andhra Pradesh (State), from July-2010 to till date.Previous Experience :
Having 2.9 years experience in “Deccan Phytochemicals” as a Assistant Chemist in Quality Assurance department at location Patancheru, Medak (Dt), from Aug-2007 to June-2010.Role and Responsibilites :
1. Sponsored links :
Responsible for maintaining the Master list of Documents, issuance of documents.
2. Responsible for preparation and review of Standard Operating Procedure (SOPs).
3. Responsible for review of executed batch production records, batch cleaning records.
4. Responsible to review the deviations.
5. Responsible for preparation of Annual product review reports for each product of APIs.
6. Responsible for reviewing of change control requests.
7. Perform the internal audits program, including preparation of annual audit plans, executing according to the plan.
8. Follow up and Execution of validation activities and review of protocols and reports. Having knowledge on validations. (Process validation.)
9. Preparation of validation protocols and reports (like Process validation)
10. Preparation for master batch production records and batch cleaning records.
12. Document controlDate :Place :
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