Louis Jeyaraj is a qualified expert, that works in SST Corporation main office of which is in 28. on the position of Executive Director, Regulatory and Technical Affairs since 2012. Louis Jeyaraj has earned professional experience in more than eight positions at various companies. Louis Jeyaraj went to the University of London and received education there from 1977 to 1982. Bridgewater, New Jersey is the area, where this expert was known to be located. This expert's contacts are easily accessed through SoftwareOfficial by request.
Name variants:
Lou Jeyaraj,
Louie Jeyaraj
Contact Information
Last Update
Jul 13, 2022
Email
lj**@sst-corp.com, si**@optonline.net
Location
Bridgewater, NJ
Company
SST Corporation
Workplace
Executive Director, Regulatory and Technical Affairs
Work History
Executive Director, Regulatory and Technical Affairs
Clifton, NJ
Oversee all aspects of SST's Regulatory & Technical Department. Responsible for assuring that SST's many API suppliers (DMF Holders) are in compliance with cGMPs and Drug Listing Require...
from Jan 2012
Regulatory CMC Manager
Successfully submitted numerous CMC submissions including complex Prior Approval Supplements and Type II variations globally involving registration of new processes (cost effective and green...
Jul 2006 — Jan 2012
Research Advisor
Developed/validated analytical methods for new product development and marketed products (reformulations, APIs and intermediates).
Provided analytical support for R&D and manufacturing/...
Feb 2004 — Jul 2006
Technical Leader
Supported quality operations analytical laboratory and chemical manufacturing (Holland, Singapore and Ireland facilities) through developing/upgrading analytical methods for drug substances,...
Jun 1996 — Jan 2004
Senior Scientist/Chemistry Manager
Managed the analytical development group (3 MS/BS chemists) and quality control group (7 MS/BS chemists).
Provided troubleshooting support for production and quality assurance problems
Respo...
Mar 1995 — May 1996
Analytical Development Group Leader
Developed and validated numerous analytical methods using HPLC, GC, GC/MS, TLC, and other techniques for the analysis of drug substances, intermediates, in-process samples, stability samples...
Jul 1991 — Mar 1995
Senior Analytical Research Chemist
Developed and validated numerous HPLC, GC, GC/MS, FT-IR, UV, and other analytical methods for the formulation development of radio pharmaceuticals and iodinated contrast media.
Characterized...
Jul 1987 — Jul 1991
Visiting Assistant Professor / Post-doctoral fellow
Jan 1982 — Jan 1987
Education
1977 — 1982
1972 — 1976
Occupations
Executive
Chief Executive Officer
Sales Specialist
Supplier
Manager
Partner
Writer
Author
Corporate Executive
Chief Executive
Services Professional
Sales Representative
Operations Manager
Skills
Gmp
Fda
Technology Transfer
Regulatory Affairs
Analytical Chemistry
Sop
Hplc
Chemistry
R&D
Glp
Regulatory Submissions
Quality Assurance
Organic Chemistry
Lc Ms
Chromatography
Mass Spectrometry
Manufacturing
Purification
Pharmaceuticals
Cgmp
Product Development
Research
Process Improvement
Process Validation
Process Development
Problem Solving
Six Sigma
Compliance
Analysis
FAQs about Louis Jeyaraj
What's the main profession of Louis Jeyaraj?
Louis Jeyaraj is a Executive Director, Regualatory and Technical Affairs.
What are the profession of Louis?
These person's professions are Executive and Chief Executive Officer
Where does Louis Jeyaraj live?
Bridgewater, New Jersey is the place where Louis Jeyaraj lives
What is Louis Jeyaraj's email?
Louis's email is lj**@sst-corp.com and si**@optonline.net.
Where did Louis Jeyaraj work?
This person worked at SST Corporation, Pfizer.
What education does Louis Jeyaraj have?
Louis studied at the University of London from 1977 to 1982.
What is professional industry that Louis Jeyaraj worked in?
Louis Jeyaraj works in Pharmaceuticals industry.
Are there any skills Louis Jeyaraj has?
This professional has the following skills: Gmp, Fda, Technology Transfer, Regulatory Affairs, Analytical Chemistry, Sop, Hplc, Chemistry, R&D, Glp, Regulatory Submissions, and Quality Assurance.