Quality Control Human Resources
Resume:
Vanitha Sajja
Solon, OH - ****9
E-mail : actdq9@r.postjobfree.com
To
The Manager
Human Resources.
Dear Recruiter,
Sub: Application for a suitable position in QC/R&D.
I am writing to express my interest in the position of Analytical Chemist and enclosing my resume outlining my qualifications and experience for your review and consideration.
I have an excellent working experience of 5 years in pharmaceutical industry. My credentials include M.Sc with specialization in Organic Chemistry. During my tenure I have performed in-process tests, conducted stability studies and gained vast experience in handling analytical instruments such as HPLC, UV, KF, Dissolution test apparatus and also acquired good QA documentation skills. I have strong aptitude for working with analytical instruments and extensive experience with computer software applications related to analytical instruments.
My ability to work with a team has contributed to my past success and guarantees my future contributions. I believe that my skills and ability will enhance the company’s success and thereby my own growth.
Thank you for your time and consideration.
Yours Sincerely,
Vanitha Sajja.
Vanitha Sajja
6645 Winston Lane, Solon, Ohio 44139
actdq9@r.postjobfree.com Page 1
Profile
Analytical chemist with skills and expertise in the following areas:
In-process, finished products and stability testing;
Method development and validation;
Instrumental calibration;
HPLC, UV-VIS Spectrophotometer, Karl Fischer titrator and dissolution test apparatus
including manual and automated dissolutions;
One media and two media dissolutions;
ANDA, process optimization and technology transfer projects;
Troubleshooting of the problems concerned with instruments and techniques;
Proficient in following written procedures, SOP’s and GLP requirements;
Documentation as per GMP, GLP and other regulatory requirements;
Laboratory information management system (LIMS) software;
MS Office Suite.
Professional Experience
2003-2005 Apotex Inc., Toronto, Canada
Level 2 Chemist, Formulation Development (R&D) (2004 – 2005)
Tested wide variety of finished products and formulations to the specific requirements of pharmacopoeias and in-house specifications which include dissolution, assay by HPLC and UV, content uniformity and blend uniformity testing.
Worked on method development and validation.
Conducted manual and automated dissolutions using Chemstation software.
Performed one media and two media dissolutions.
Worked on ANDA and Process Optimization projects.
Well trained in handling Special Products (high potent drugs) under controlled premises.
Efficiently met project deadlines while complying with GMP.
Actively participated in team oriented projects.
Level 1 Chemist, Analytical Research & Development and Product Evaluation (ARD-PE) (2003-2004)
Tested finished products using HPLC, Karl Fischer and Dissolution test apparatus.
Effectively involved in the analysis of Initial and Stability samples.
Worked in accordance with approved methods: SOP’s, GMP and GLP.
Involved in the operation and trouble shooting of analytical instruments such as HPLC, UV, KF and Dissolution test apparatus.
Performed one and two media dissolutions using Perkin Elmer (PEDS) and Chemstation softwares.
Hands on experience in using Vankel VK 2000 Automated Dissolution.
Conducted In-process and Physical tests.
Worked on Technology Transfer projects.
Wrote detailed analytical reports and acquired good QA documentation skills.
Vanitha Sajja Page 2
1999-2002 Endoven Products, Hyderabad, India
Quality Control Chemist
Tested and interpreted results of Active Pharmaceutical Ingredients (API).
Calibrated and maintained analytical instruments as per schedule.
Tested finished products using HPLC, UV Spectrophotometer and Dissolution test apparatus.
Determined the water content of raw material and finished products by loss on drying (LOD) and Karl Fischer moisture titrator.
Conducted and evaluated stability studies.
Input of analytical results into Stability Data Report.
Assisted in developing and validating new analytical methods to suit in-house specifications.
Professional Development
2002 SRN Professional Training Center, Toronto, Canada
Completed six-month Pharmaceutical Quality Control Training Program.
2002 Seneca College, Toronto, Canada
Upgraded skills in quality assurance and laboratory assay methods by HPLC and UV spectrophotometer.
2001-2002 Teena Labs Private Limited, India
Trained in HPLC using chromcard software
Education
Master of Science in Organic Chemistry, Osmania University, India.
Bachelor of Science in Microbiology, Genetics and Chemistry, Osmania University, India.
References Available Upon Request
Contact this candidate