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Rajendra C

Pharmaceutical Scientist

Occupation:

Quality Coordinator

Location:

Clifton, NJ

Education Level:

Master

Will Relocate:

No

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ver fifteen years of solid experience in pharmaceutical Quality Assurance, Quality Control, Stability, Analytical methods development, Validation, Instrumentation, Lab supervisor and Academic. Accomplished, results-oriented individual with expertise in pharmaceutical area. Extensive hands on experience with HPLC, TLC, GC, TGA, UV/VIS, FTIR, IR, AA, Fluorescence Spectrophotometer and Dissolution. Up-to-date knowledge of cGMP and cGLP compliance requirements. Skilled at performing a variety of routine and non–routine complex scientific tests utilizing laboratory apparatus, including an analytical analysis and recording of data.

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COMPANY POSITION HELD DATES WORKED

Amneal Pharmaceuticals Scientist III 11/2017 - 2/2018
Sunrise Pharmaceuticals Analytical R&D Chemist 1/2016 - 11/2017
scientech Laboratories Analytical R&D Chemist 8/2015 - 1/2016
Novartis Pharmaceuticals Group Leader 2/2000 - 10/2011
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SCHOOL MAJOR YEAR DEGREE

Stevens Institute of Technology Instrumentation Chemistry 1998 Master Degree
B.K.M Science Clooege, INDIA Organic Chemistry 1984 Master Degree
B.K.M. Science college, INDIA Chemistry 1982 Bachelor Degree
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TYPE TITLE URL DESCRIPTION

Book Pharmaceutical Technology media url Pharmaceutical
Book GEN media url Biotechnology
Magazine Scientific media url HPLC-GC

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Highlights:

Companies I like:

J&J, Celgene, Merck

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• Conducted method development and method validation activities using GC, HPLC, Particle size analyzer, Karl Fischer and other wet chemistry techniques. • Designed method validation strategy, review validation protocol and completion report. Troubleshoot analytical instrument and test method • Conducted analytical research and developed methods to test pharmaceuticals products to established specifications. • Performed analytical testing of R&D batches, Stability batches, cleaning validation samples and generated final analysis report. Familiar with cGMP, FDA / ICH guidelines and OSHA regulations. • Good analytical, administrative, organizational and supervisory skills. Problem solving and decision making ability. Strong multitasking skills. • Fast learner and computer literate. Flair of getting things done and able to work efficiently and productively. • Managed administrative functions in the absence of the Manager.
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