Resumes
Resumes
![Jason Teelucksingh Photo 1 Jason Teelucksingh Photo 1](/img/not-found.png)
R And D And Manufacturing Lead
View pageLocation:
109 Zwolak Ct, South Plainfield, NJ 07080
Industry:
Pharmaceuticals
Work:
Halo Pharmaceutical, Inc. Jun 2012 - May 2013
Project Manager
Apex Pharmaceuticals, Inc. 2013 - 2013
R and D and Manufacturing Lead
Novartis Dec 2001 - Jun 2012
Senior Scientist Formulation Development
Gsk Jun 2000 - Dec 2001
Analytical Development
Eon Labs Jan 1992 - Jun 1999
Analytical Development
Project Manager
Apex Pharmaceuticals, Inc. 2013 - 2013
R and D and Manufacturing Lead
Novartis Dec 2001 - Jun 2012
Senior Scientist Formulation Development
Gsk Jun 2000 - Dec 2001
Analytical Development
Eon Labs Jan 1992 - Jun 1999
Analytical Development
Education:
Long Island University 1996 - 2003
Master of Science, Masters, Pharmacy Hunter College 1988 - 1992
Bachelors, Bachelor of Science, Chemistry
Master of Science, Masters, Pharmacy Hunter College 1988 - 1992
Bachelors, Bachelor of Science, Chemistry
Skills:
Hplc
Analytical Chemistry
Lc Ms
Project Management
Quality By Design
Cleaning Validation
Teamwork
Process Optimization
Project Planning
Budget Monitoring
Formulation Development
Budget Forecasts
Equipment Qualification
Process Development
Nir
Gc/Ms
Methods Development
Process Validation
Pharmaceutical Industry
Gmp
Technology Transfer
Research and Development
Validation
Formulation
Standard Operating Procedure
U.s. Food and Drug Administration
Good Laboratory Practice
Regulatory Affairs
Drug Development
Pharmaceutics
Product Development
Chromatography
Clinical Development
Quality Assurance
Corrective and Preventive Action
Manufacturing
Cross Functional Team Leadership
Change Control
Regulatory Submissions
Management
Quality System
Cro Management
Analytical Chemistry
Lc Ms
Project Management
Quality By Design
Cleaning Validation
Teamwork
Process Optimization
Project Planning
Budget Monitoring
Formulation Development
Budget Forecasts
Equipment Qualification
Process Development
Nir
Gc/Ms
Methods Development
Process Validation
Pharmaceutical Industry
Gmp
Technology Transfer
Research and Development
Validation
Formulation
Standard Operating Procedure
U.s. Food and Drug Administration
Good Laboratory Practice
Regulatory Affairs
Drug Development
Pharmaceutics
Product Development
Chromatography
Clinical Development
Quality Assurance
Corrective and Preventive Action
Manufacturing
Cross Functional Team Leadership
Change Control
Regulatory Submissions
Management
Quality System
Cro Management
![Jason Teelucksingh Photo 2 Jason Teelucksingh Photo 2](/img/not-found.png)