
Assistant Manager at Johnson & Johnson
India

Assistant Manager at Johnson & Johnson
India
The woods are lovely, dark and deep,
But I have promises to keep,
And miles to go before I sleep,
And miles to go before I sleep.
These are the words by Robert Frost. Nothing better can sum up my atitude towards life. I have always wanted to learn something new everyday.
I am a Veterinary Pathologist having done my M.V.Sc in Pathology from Madras Veterinary College. After my graduation, I moved into my passionate field, Toxicologic Pathology. I always enjoy my work in this territory and I try to excel in industrial research.
Now with a varied experience in drug, biological and consumer product toxicology I can only say humbly that as is the case with everybody, the number of unknown facts would far exceed the known facts. I try to bridge the gap always.
Toxicologic Pathology, Toxicology, Non-clinical drug development
(Public Company; JNJ; Pharmaceuticals industry)
August 2009 — Present (5 months)
(Privately Held; Biotechnology industry)
August 2007 — July 2009 (2 years )
GLP Certified lab)
-Perform various regulatory toxicity studies as per GLP principles.
- Preparation of study protocol and ensure timely conduct of studies
- Interpret findings and preparation of study reports
- Prepare summary reports for regulatory submissions
- Perform the routine histopathological screening and interpret the results of the toxicity studies.
-Perform the interpretation of clinical pathology data.
-Perform DLC, Reticulocyte and Bone marrow smear analysis
(Public Company; 10,001 or more employees; Pharmaceuticals industry)
June 2004 — August 2007 (3 years 3 months)
(GLP Certified lab)
- Perform histopathological screening, correlation & interpretation the results & prepare reports.
- Perform haematology and clinical chemistry analysis & interpretation of clinical pathology data.
- Perform DLC, Reticulocyte and Bone marrow smear analysis and their interpretation.
- Perform various regulatory and non-regulatory toxicity studies as per GLP principles.
- Serve as a Study Monitor for various studies outsourced and identification of CROs for toxicity studies.
- Visited RCC Labs, Switzerland to monitor the critical phases of the IND directed studies of NCEs.
- Preparation of study protocol and ensure timely conduct of studies.
- Interpret findings and preparation of study reports.
- Prepare summary reports for regulatory submissions.
- Co-ordinated and conducted regulatory studies for four IND molecules.
- Assist in the preparation of the pharmacology/toxicology sections for annual reports, IBs, INDs.
(Research industry)
May 2003 — June 2004 (1 year 2 months)
(GLP Certified lab)
- Interpret findings and preparation of study reports
- Prepare summary reports for regulatory submissions
- Perform the routine histopathological screening and interpret the results of the toxicity studies.
-Perform the interpretation of clinical pathology data.
-Perform DLC, Reticulocyte and Bone marrow smear analysis
M.V.Sc , Veterinary Pathology , 2000 — 2002
B.V.Sc , Veterinary Sciences , 1994 — 2000
Owner and Moderator of E-Society of Toxicologic Pathology (http://groups.google.co.in/group/toxicologic-pathology?hl=en)
Full Member of Society of Toxicologic Pathology
Life Member of Society of Toxicologic Pathology of India
Life Member of Indian Association of Veterinary Pathologists
Senior Member of Science Advisory Board
Stood among Top 5 in the B.V.Sc class.
Recepient of TANUVAS Merit Scholarship to pursue M.V.Sc in Veterinary Pathology.
Stood among Top 5 in M.V.Sc class.
Awarded Full Membership of Society of Toxicologic Pathologists, USA and a Full Member of the same society since 2004.