Validation Consultant (Through Kelly Services) @ •Collect and analyze data from executed production batch records, development reports, qualification reports, in-process and finished product certificate of analysis, other manufacturing sites for investigation, process evaluations, and validation activities. •Write process validation protocols, validation and technical reports, amendment, and validation assessment for the manufacturing of Consumer Healthcare Products. From March 2012 to July 2013 (1 year 5 months) Richmond, Virginia AreaValidation Scientist III @ •Utilize bracketing and worst case strategy to develop and execute cleaning, and equipment validation programs. •Write and execute approved process validation and performance qualification protocols for manufacturing, compression, and packaging processes. From May 2006 to September 2008 (2 years 5 months) Associate Scientist II @ •Prepare and review technical protocols, reports, and other technical documents to support process and cleaning validation projects and activities. •Compile, maintain, and update process and cleaning validation timelines. •Write and execute process validation protocols, report, amendment, and validation assessment for the manufacturing of Liquids, Creams, Ointment, Capsules, and Tablets. •Conduct process validation protocol and report review sessions for protocol and report approval. From April 2000 to May 2006 (6 years 2 months)

Master’s Degree @ Kean UniversityBachelor’s Degree @ Rutgers, The State University of New Jersey-Newark Nat Boateng is skilled in: SOP, Change Control, Validation, Cleaning Validation, GMP, R&D, Pharmaceutics, FDA, CAPA, Pharmaceutical Industry