Quality Control/ Analytical chemist
Resume:
Juhi Bhatt **** Stage road
****.******@*****.*** Buena Park, CA.
STRENGTH
• Strong knowledge of Analytical techniques, Data processing software and Strong computer skills.
• Excellent handling and Method development skills with UPLC, HPLC, UV-VISIBLE Spectroscopy, AAS, GC, FTIR, TLC, Dissolution apparatus
• Experienced with the formulation of Solid Novel Drug Delivery System with knowledge to improve formulation and process to increase efficiency.
• FDCA Approved chemist
• Sound experience of all Analytical and Physical Testing techniques of Raw Materials, Bulk and Finished Products, R&D Products and Stability studies of Solid, Semisolids, Liquids and Aerosols.
• Sound knowledge of Pharmacokinetics, Pharmacodynamics, Pharmacology and Targeted Drug Delivery systems.
• Experience with FDA, and cGMP, regulations and guidelines.
• Expertise with the Quality control analysis, Quality control calculations, preparation of standards and dilution, Wet chemistry techniques.
• Good Communication & Presentation Skills and Open to new ideas and adapting changes in work environment.
PROFESSIONAL EXPERIENCE
Analytical Chemist
GORDON Laboratories, Carson, CA 90746
March 2018 to present
• Perform analytical testing of Raw Materials, In Process Bulk and Finished Products for Active Pharmaceutical Ingredients (API) in over the counter (OTC) personal skin care product.
• Development, Optimization and Validation of Analytical method using HPLC, GC, and AAS.
• To perform the Batch Formulation, Optimization and Evaluation of Creams, Sunscreen Lotion, Shampoo, Toothpaste, Mouthwash, Exfoliating solutions and stick in the R&D Department.
• Monitor the calibration of Viscometer, Melting point apparatus, pH meter, Weighing Machine, HPLC, GC, AAS, FTIR, Refractometer
• Review Micro testing and Physical testing for all the materials executed by Lead Physical chemist and Lead Microbiologist.
• To review and release COA of Raw Materials, Bulk and Finished Products .
• Prepare and Review QL and MSDS of Raw materials and finished products. Senior Quality Control Chemist
Supra Drug and Food Testing & Research Laboratory, Gujarat, India.
(Approved By FDCA, Gujarat, INDIA. LIC.NO.GTL/37/34) August 2015 to December 2017
• UHPLC Method development, analysis and validation of finished product, stability samples and raw materials using Chromeleon Software including assay & related substances with respect to pharmacopoeias
• Trouble Shooting of Equipment Like UHPLC, UV & IR During Process
• Perform hands-on wet lab work to develop new workflows and assays or validate assays on existing and new instrumentation platforms
• Plan, execute, analyze and troubleshoot laboratory work related to analytical/pharmaceuti- cal development
• Independently plan, execute and manage projects/programs that both span multiple disci- plines and utilize established methods, techniques or approaches
• Provide oversight of junior-level Development colleagues to execute experimental and ana- lytical testing.
• Use scientific expertise to provide assistance to coworkers for troubleshooting Quality Control Chemist
Supra Drug and Food Testing & Research Laboratory, Gujarat, India.
(Approved By FDCA, Gujarat, INDIA. LIC.NO.GTL/37/34) November 2013 to August 2015
• Executed analysis of chemical products using United States Pharmacopoeia (USP) and SOPs and in-house testing methods utilizing HPLC, TLC, UV and wet chemical techniques
• Performed stability testing, dissolution by HPLC and dissolution by automated UV
• Responsible For Following All Relevant SOP, Safety and Company Guidelines
• To Maintain Logbook, Protocols and Documents Related To Instrument Lab with respect to GDP
• Perform testing, both wet and instrumental, according to SOP’s testing protocols, or compendia (USP EP/JP)
• Calibration of PH meter, Polari meter, Dissolution Apparatus, IR Spectroscopy, Weight balance, Melting point apparatus, Viscometer.
ACADEMIC QUALIFICATION
Masters of pharmacy (Ranked 2nd in State University) (2012-2014)
(Pharmaceutical Technology) (CGPA: 8.74)
APMC College of Pharmaceutical Education & Research, Gujarat Technological University, India
Studies Included: Pharmaceutical Formulation Development & Biopharmaceutics, Experimental Design and Patents, Novel Drug Delivery system, Modern analytical technique, Industrial Pharmacy Practice, Research Methodology, Global Regulatory Requirements. Masters of Business Administration (Distinction)
Dr. C. V. Ramen University, India.
Registered Licensed Pharmacist (G50274)
Gujarat State Pharmacy Council, India.
Bachelors of pharmacy (CGPA: 8.20) (2008-2012 )
APMC College of Pharmaceutical Education & Research, Gujarat Technological University, India
Studies Included: Pharmaceutical Engineering, Dosage Form Design, Pharmacognosy, Pharmaceutical Technology, Anatomy Physiology and Health education, Pathophysiology, Organic chemistry, Pharmaceutical Microbiology, Medicinal Chemistry, Analytical Chemistry, and Pharmacology.
RESEARCH TOPIC
“DESIGN DEVELOPMENT AND EVALUATION OF SUSTAINED RELEASE DOSAGE FORM OF ZIDOVUDINE (ANTI-HIV DRUG) USING MICRO-PARTICULATE SYSTEM” During research and development work on Micro particulate system using Anti-Retroviral drug named ZIDOVUDINE the first ever FDA approved drug as an Anti HIV agent and developed a Sustained release Microspheres of Zidovudine drug with different polymers to reduce the administration of capsules or tablets in a day including its Physical and Analytical tests development.
WORKSHOP/TRAINING ATTENDED
• Participated In 63rd Indian Pharmaceutical Congress Held At Bangalore International Exhibition Center during 16th-18th December 2011 at Bengaluru, India.
• Attended AICTE Sponsored One Day National Seminar On “Pharmacovigilance And Clinical Trials In Developing Countries: Challenges And Opportunities” Held At Shri B.M Shah College Of Pharmaceutical Education & Research during July 20, 2013.
• Attended workshop on Patenting in Pharmaceuticals sponsored by AICTE New Delhi, India
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