shikha bist, Drug Regulatory Affairs

shikha bist

Drug Regulatory Affairs

Kuwait Saudi Pharmaceutical Industries Company

Location
United Arab Emirates - Abu Dhabi
Education
Doctorate, Chemistry
Experience
6 years, 0 Months

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Work Experience

Total years of experience :6 years, 0 Months

Drug Regulatory Affairs at Kuwait Saudi Pharmaceutical Industries Company
  • Kuwait
  • December 2012 to August 2016

Preparation, Compilation & Submission of Drug dossiers in CTD or NeeS format to local and foreign regulatory authorities like GCC nations: KSA, Bahrain, Qatar, UAE, Oman and Non GCC nations: Jordan, Iraq, Ethiopia etc.

New registration of drug product to procure marketing approval in different countries, submitting re-registration and minor variations documents.

Coordinate with our agents in different countries to meet national and international regulatory requirements and guidelines.

Managing Chemistry Manufacturing and Control (CMC) aspects to prepare the corresponding Quality related dossiers for registration.

Updating Information regarding domestic, GCC and International guidelines or standards needed for Drug Product registration.

Liasing with heads of different departments like QC, QA, Sales, Purchase and Production in handling technical queries and arranging Quality related technical information and documents .

Chemistry Lecturer at Jyoti Vidyapeeth Women University
  • India - Jaipur
  • December 2010 to June 2011

Delivering lectures and conduct laboratory experiments.evaluate student performance .Planning strategies to enhance student's learning capabilities.

Analytical Development Chemist at Sterling Biotech Ltd
  • India - Vadodara
  • June 2007 to January 2009

Analytical method development of Active Pharmaceutical Ingredients using modern analytical techniques e.g HPLC, GC, UV-Visible, FT-IR Spectroscopy, DSC, Gravimetric analysis.Wet lab analysis, analysis of raw material, in-process and finished product samples as per required standard. Instrument calibration and maintenance and ensure that laboratory records /documentation comply with cGMP.To work in compliance with company and regulatory requirements.

Education

Doctorate, Chemistry
  • at University of Rajasthan, Jaipur
  • August 2007

Synthesis of novel derivatives of terpenoids.Synthesis and isolation of binary and ternary complexes with biologically active metals and amino acids.Physicochemical studies to establish stoichiometry of complexes by potentiometric,spectrophotometric and spectroscopic studies and elemental anlalysis.Biological investigation of synthesized complexes.

Doctorate, Chemistry
  • at University of Rajasthan
  • January 2007

• Ph.D. Chemistry -2007, Department of Chemistry, University of Rajasthan, Jaipur, India. Thesis entitled "Physicochemical and Biological Studies of Ternary Complexes of some Terpenoids and their Derivatives".

Master's degree, Chemistry
  • at University of Rajasthan
  • January 2001

Masters in Chemistry with Specialization in Organic Chemistry

Bachelor's degree, Chemistry, Botany and Zoology
  • at Maharani College, University of Rajasthan
  • January 1999

• Bachelor in Science with subjects : Botany,Zoology and Chemistry.

Specialties & Skills

Organic Chemistry
HPLC,GC,UV,FTIR Spectrometer,DSC and other modern analytical instruments
writing and maintenance of SOP and technical documents
CTD,eCTD, GMP,GLP
MS Word, Excel, Power Point ,Window 2007
ATOMIC ABSORPTION
CALIBRATION
CHEMISTRY
DERIVATIVES
DOCUMENTATION

Languages

Hindi
Expert
English
Expert

Training and Certifications

P.G. Diploma in Patents Law (Certificate)
Date Attended:
April 2010
Valid Until:
April 2012
P.G. Diploma in Pharma Regulatory Affairs (Certificate)
Date Attended:
December 2011
Valid Until:
August 2012
CTD-Drug master file compiling (Certificate)
Date Attended:
August 2012
Valid Until:
August 2012