MADUNALA NAVEEN KUMAR
+1-918-***-****, Jersey City, NJ
E-mail: *************@*****.***
SUMMARY:
3+ years of experience in chemistry field, as a Research Associate, production officer and Teaching Assistant in various positions.
Maintaining ISO (International Organization for Standardization) and cGMP (Current Good Manufacturing Practice) guidelines.
Hands on experience in dealing with method development and validation of drug substances and drug products.
Performing a variety of routine and complex analytical tests using, HPLC, UV, FTIR, Dissolution, Karl-Fisher Tiltrotor and Polari meter.
Accurate pharmaceutical calculations (Molality, Morality, yield value, initial and final concentration, percentage, dilution factor calculations) and statistics (mean, average, standard deviation, rejected and accepted value)
Assist with the maintenance, review, reporting and verification of documents including analytical data, analytical notebooks etc. in compliance with the SOPs.
Problem-solving skills, ability to work within an interdisciplinary team, and excellent oral and written communication.
Strong interactive skills with in cross-functional teams to successfully drive the project forward
Proven as a efficient production officer with meet production deadlines on time and every time.
High adopted to manufacturing circumstances with good man power management.
Efficient in performing troubleshooting within method guidance.
PROFESSIONAL EXPERIENCE:
Southeast Missouri State University, Cape Girardeau Jan 2015 – May 216
Teaching Assistant, Analytical and Organic Chemistry Courses
Instructor on B.S. degree students on wet chemistry such as
Titration
Sample extraction
Supervised and instructed undergraduate students in the Organic Chemistry laboratory courses
Graded Organic Chemistry course examinations and laboratory reports and delivered problem solving sessions in place of the Organic Chemistry course instructor
Dr. Reddy’s Laboratories Ltd Hyderabad, India
Research Associate December 2012 – June 2014
Responsibilities:
Analytical method development and validations for drug substances (assay, related substances).
Preparation of analytical method validation protocol and execution of the analytical method validation and prepare validation reports for drug substances.
Develop and validate cleaning methods by UV and HPLC for intermediates and API.
Operation and performance verification of instruments like Analytical Balance,
Microbalance, pH Meter, Incubated shaker bath, Deep freezers (-65 C, -20 C), Cooling
Cabinet (2-8 C), Vibramax platform shaker, Solid Phase Extractor, HPLC.
Routine day to day analysis in Wet lab.
Calibrations of instruments as per SOPs.
Maintaining Good Laboratory Practices (GLP) and Documentation
Asian Paints, Solvent Paint Department Hyderabad, India
Production Officer August 2011 - November 2012
Responsibilities:
Deployed the work to the operators as well as encourage them to reach production as per schedule.
Looking after production along with safety and quality. Batches planning as per customer requirements, man power deployment for each shift, working on section parameters, and ensuing compliance against GMI.
In depth knowledge on production process, and supporting systems for ensuring target achievement. Man power management which is key for a large scale production companies, importance and requirements of carrying ISO certification. Methods of production streamlined operations.
EDUCATION:
Masters of Science, Chemistry Aug 2016
Southeast Missouri State University, USA
Masters of Science, Analytical Chemistry April 2011
OSMANIA University, Hyderabad, INDIA
Bachelor of Science, Bio Technology and Chemistry, April 2008
OSMANIA University, Hyderabad, INDIA
Certifications:
FEMA (Federal Emergency Management) Certificate, USA
SAS ( Basic) Certificate, India
ACADEMIC RESEARCH:
Photo and magnetic actuation of IA-CNTS for treating cancer cells by hyperthermia