Biodata |
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| Name of the Candidate | : | [Private] |
| Name of the Post Applied | : | Drug Regulatory Affairs Executive |
| Job related skills / software | : | Early stages of Drug Discovery, Development and Approval process for Global Regulatory Market, Knowledge on US FDA, EMA, ICH, WHO, OECD guidelines, Dossier compilation and submission of DMF, ASMF, ANDA, IND, CTA, NDA, MAA, to various regulatory authorities across the world. |
| Category | : | Medical |
| Sub Category | : | Drug Regulatory Affairs Executive |
| Years of Experience | : | 0 years |
| State | : | Andhra Pradesh |
| Gender | : | Male |
| Salary Expected per Month(Rs) | : | Negotiable |
| Highest Qualification attained | : | M.S. / MS : Master of Science |
| Major / Specialization | : | Regulatory Affairs and Drug Development |
| Email Id | : | [Private] |
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| Are you looking for job now? | : | Yes |
| Can the recruiter contact you? | : | Yes |
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SATHISH KUMAR THADAM
Email :sathishthadam87 AT gmail.com
Phone : (+91)-8374222313
OBJECTIVE :
To obtain a position that promotes individual opportunity and professional growth in Regulatory Affairs and Drug Development while making positive contribution to the organization.
EDUCATIONAL QUALIFICATION :
COURSE DURATION UNIVERSITY/BOARD COLLEGE PERCENTAGE M.S. in Regulatory Affairs and Drug development 2011-2013
JNTU Hyderabad Alliance Institute of Advanced Pharmaceutical and Health Sciences 73%
B. Pharmacy 2007-2011 Kakatiya University, Warangal S.R College of Pharmacy, Warangal. 67%
Intermediate 2002-2004 Board of Intermediate Education, A.P Millennium junior college, Karimnagar 70%
SSC 2001-2002 Board of Secondary Education, A.P Gouthami High School, Jammikunta 75%
TECHNICAL SUMMARY :
Early stages of Drug Discovery, Development and Approval process for Global Regulatory Market.
Knowledge on US FDA, EMA, ICH, WHO, OECD guidelines.
Dossier compilation and submission of DMF, ASMF, ANDA, IND, CTA, NDA, MAA, to various regulatory authorities across the world.
WORK EXPERIENCE :
Have done project in, HETRO Labs Limited Hyderabad on “Paediatric Regulations, Compilation of Module 2 CTD for Europe, United States and India ” for the period of 6 months.
Worked in HETRO
Labs Limited as a intern in Drug Regulatory Affairs Dept from November 2012 – May 2013.
Actively involved in dossier preparation of CTD for USA and EU countries and African Countries (ROW).
SKILLS :
Compilation of DMF, ANDA, NDA, CTA, etc.
Having sound knowledge in global regulatory affairs.
Good computer skills in MS Office, MS Word and PDF.
INTRESTED AREAS :
Regulatory affairs.
Pharmacovigilance.
Quality Assurance.
Drug Development.
EXTRA CURRICULAR ACTIVITIES :
Participated in various cultural events held in college.
Successfully presented a poster in IPC64 at Chennai.
An oral presentation on GDUFA in RIPE in JNTU at Hyderabad.
STRENGTHS :
Positive outlook.
Self starting with high energy levels.
Good leadership qualities.
Excellent communication skills
Interest to take up new challenges and learn new things.
PERSONAL PROFILE :
Name : SATHISH KUMAR THADAM
Date of Birth : 8th Aug, 1987.
Languages known : English and Telugu.
Marital Status : Single.
Nationality : Indian.
DECLARATION :
I hereby assure that the information I have furnished is true to the best of my knowledge.
Date :
Place : Hyderabad
(SATHISH KUMAR THADAM)
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