Gulfjobseeker.com CV No: 1434120
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Objective
To secure a challenging & growth oriented position where my skill can be effectively utilized and improved
eventually leading to growth of the organization and myself.
Education
Degree
Year
School/College
Uni./Board
Per
M.Pharm
2013
Nargund college of pharmacy,
Bangalore
R.G.U.H.S
Bangalore
(Karnataka)
75%
B.Pharm
2010
Dayananda sagar college of pharmacy,
Bangalore
R.G.U.H.S
Bangalore
(Karnataka)
62%
H.S.C
2005
K.C Kothari Secondary & HighSecondary School
GSHSEB
51%
2003
K.C Kothari Secondary & HighSecondary School
GSEB
74%
(science Stream)
S.S.C
Skills and Competencies
Formulation & development & Drug development process
In-process checks and quality controls
ICH, GMP, GLP & GCP & WHO guidelines
Validation methods & Stability studies and documentation & record filling
Handling & operating of HPLC, UV, IR analytical Instruments and all kind of PRE & POST
FORMULATION and EVALUATION INSTRUMENTS
Strengths
Good communication skills
Independent, Honest, Sincere and Hard working
Excellent interpersonal skills, confident in interactions with individual at all levels
Organized individual with exceptional flow through capabilities
Strong coordination and management skills
Computer Proficiency
Software - MS Office (MS Word, MS Excel, MS PowerPoint)
Academic Projects
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“Preparation and Evaluation of Buccal Formulation for an Anti-Emetic Drug”
Submitted as a part of M.Pharm curriculum to the Rajiv Gandhi University of Health Sciences, Bangalore
Certification course
I completed Skills Acceleration Program successfully during 2007 to 2009 from CIL ( Centre for Innovation &
Leadership.
Training
Training under taken in title of Estimation of quantity & quality of tablets, capsules, parentrals,
liquids, orals in quality control department in “ELYSIUM PHARMACEUTICALS LTD, BARODA.
Experience
currently, I am working as Sr. IPQA Officer in Claris otsuka pvt ltd.
I was working as a IPQA with Sava Healthcare Limited (Previously known as Biodeal Laboratories Pvt. Ltd.),
Surendranagar from June/2013 to April/2015, I have successfully faced many audits of countries like
Ukraine, Uganda, Turkmenistan, Kazakhstan etc and various audits from contract manufacturers. I also
have FDA & WHO GMP audits experience.
Our plant is Manufacturing Loan License & Trading Products of companies like Lupin Laboratories Ltd., Dr.
reddy’s laboratories ltd., Sun pharma LTD., Intas Pharmaceuticals LTD, Glenmark Pharmaceutical LTD,
Macleods Pharmaceutical LTD., Abbott India LTD., Ranbaxy Laboratory LTD., Cadila Healthcare Ltd., Torrent
Pharmaceutical LTD., Bergen Healthcare (Alkem), etc, and own products for domestic market and export to
countries like Ukraine, Uganda, Mauritius, Singapore, Srilanka, UAE, Kenya, Congo, Malaysia,etc.
Previously, I worked as QC chemist at SDPARC and having knowledge about HPLC, IR, UV etc.
Current job profile
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Reporting to Q.A. Head,
Issuing of line clearance at every step of batch manufacturing,
Performing in-process quality assurance checks for Parentral products,
Authorization of Overprinting matters of PM Used For Packing & Finally Released For Market,
Maintaining and updating the Batch Manufacturing Records,
Documentation of log books, calibration records, temperature and humidity records etc.,
Assisting in process validations,
Review of BMR and BPRs
Handle investigations of Deviations,
Review of change controls related to Manufacturing activity,
Review of Master documents related to Production,
Review of artworks related to printed packing materials,
Preparation of SOP/SCP, Process Validation Protocols & Reports, APQR.
Preparation & Maintenance of Product File
Interests
R&D, Quality assurance & Corporate quality assurance.
Hobbies
Reading books, travelling and try to learn new things
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Personal information
Birth-date
6 t h feb 1988
Language Known
English, Hindi, Gujarati
Marital Status
Un-Married
Nationality
Indian
Hobbies
Playing Cricket, Reading, Music
Declaration
I hereby declare that all the information mentioned above is true to my knowledge and belief.
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