I am a dedicated, proactive and seasoned professional, acknowledged throughout my career for designing and executing comprehensive strategies for the manufacture of APIs, clinical trial materials and pharmaceutical intermediates and for overseeing the scale-up and subsequent implementation of the corresponding manufacturing procedures at a series of global CROs and CMOs. I am a high achiever with strong leadership abilities and have a history of utilizing sound technical, regulatory and QA-compliant approaches for improving the selected process chemistries and for overseeing the ensuing scale-up and technology transfer activities, ensuring that the optimized manufacturing processes are implemented in a time- and cost-effective manner.I have authored 44 peer-reviewed scientific publications and hold 14 US and/or international patents.
Listed skills include Pharmaceutical Industry, Drug Development, Technology Transfer, Gmp, and 34 others.