Senior Scientist / Team Leader Resume
P, etc) protocols and documentation
• Proficient in Thermal/Chemical Analysis (Qualitative, Quantitative)
• Strongly skilled in analytical instrumentation such as FTIR, UV-Spectrophotometer, GC, HPLC(Totalchrom / Turbochrom / Chemstation, Empower), Karl Fischer, DISSOLUTION,
• Knowledge of Microsoft Word and Excel, Method Development
• Knowledge of Method Transfer / Validation (Linearity, Accuracy, Precision, etc)
• Good communication skills, tolerant and patient with people.
• Goal Oriented and Results Driven Team Leader .
EXPERIENCE
Novartis Pharmaceuticals Corp. Jan. - Present
Senior Scientist
Analyze Solid dosage forms as per SOP, USP using HPLC, UV-Vis
Dissolution, Content Uniformity, Assay, Impurities, etc.
Documentations as per SOP, USP. cGMP, etc
Nice Pak Products Inc. Oct. - Dec.
Analytical Chemist(III) / Team Leader
Conducted analysis on stability & finished products for releases. Analyzed sample batches for Production Dept., using instrumental techniques (HPLC,UV-Vis, FTIR, GC, Auto-titrator, TOC, etc) as per monographs, USP, etc. Maintained & observed cGMPs and safety. Trained & supervised new analysts and reviewed their documentations as per SOP, USP. Represented QA Manager when FDA / OSHA visited company. Assisted QA Manager and Director. An Internal Auditor. Assisted R&D Dept. in Method Development and transfer.
Par Pharmaceutical Inc. May – Oct.
Quality Control Chemist
Performed analysis on raw material samples using classical wet chemistry and instrumental techniques (HPLC, GC, FTIR, UV-VIS, Potentiometer, Manual titration, Sonic, Air-jet, Malvern & Ro-Tap sieve analysis, Bulk & Tapped density, Karl Fischer, wet chemistry methods, packaging components, etc.). Maintained & observed cGMPs and safety. Assisted Manager & Group leader with raw material document control, filing, etc. Trained new Analysts as per SOP and USP. Reviewed analysts’ notebooks.
EDUCATION
Long Island University, Brooklyn, NY.
MS in Industrial Pharmacy, May
BS in Chemistry, May
