Jayesh Narola is a high-skilled expert, who works in Nostrum Laboratories on the position of Project Lead, Analytical R&D from 2012. This person gained professional experience in more than six positions at various companies. Jayesh Narola went to the Long Island University, Brooklyn Campus and received education there from 2007 to 2009. This expert has such qualifications as Lean Six Sigma Green Belt, Six Sigma Global Institute, License Accredible-10377394, and License Accredible-10377394. Philadelphia, Pennsylvania is the city, where the professional was lastly known to be located. This professional's email address and phone can be easily accessed through this website by request.
Name variants:
Jayesh Narola
Last updated Apr 12, 2024
Contact Information
Last Update
Jun 22, 2022
Email
jb**@gmail.com
Location
Philadelphia, PA
Company
Nostrum Laboratories, Inc
Workplace
Project Lead, Analytical R&D
Work History
Project Lead, Analytical R&D
NOSTRUM LABORATORIES, INC.
Plan and assign job responsibilities to research associates for timely release of raw materials, in-process, finished products, excipients and other materials supporting R&D analytical...
from Jan 2012
Chemist 1
Kansas City, Missouri Area
Reviewed laboratory tests after proper analyzing, documentation, and reported data findings while adhering to compliance
Performed phosphate binding study for ANDA submission and wrote ...
Jan 2011 — Dec 2011
Analytical R & D Associate
Kansas City, Missouri Area
Prepared validation protocol for Cleaning Verification as well as data collection and documentation review
Executed Intermediate Precision study
Wrote reports and conducted CAPA (Corre...
May 2010 — Dec 2010
Pharmacy Manager
Buffalo/Niagara, New York Area
Applied drug inventory management System to reduce waste
Consulted on medication dosage, interactions, disease management and potential side effect with physicians and patients
Attende...
Feb 2010 — Apr 2010
R&D Associate-Formulation
Ahmedabad Area, India
Executed feasibility batches
Supported product transfers from R&D to Production, conduct training
Coordinated with regulatory affairs department for document and SOP approval and...
Feb 2006 — Jun 2006
Production Intern
Ahmedabad Area, India
Acquisitioned and dispensed Raw material
Maintained proper batch records, documented and validated instruments as well kept organized data base of Raw materials and finished products
E...
Nov 2005 — Feb 2006
Education
2007 — 2009
2003 — 2005
2000 — 2001
Occupations
Executive
Senior Manager
Accountant
Accounts Receivable
Project Manager
Scientist
Chemist
Operations Manager
Project Managers
Skills
Gmp
Validation
Pharmaceutical Industry
R&D
Formulation
Sop
Glp
Pharmaceutics
Hplc
Regulatory Affairs
Capa
Standard Operating Procedure
Quality Control
Dissolution
Fda
Quality Assurance
Software Documentation
Biotechnology
21 Cfr Part 11
Change Control
Regulatory Submissions
Good Laboratory Practice
Analysis
Research
Quality System
Data Analysis
Ic
Research and Development
High Performance Liquid Chromatography