Kashiv Pharma, LLC. is an emerging pharmaceutical research and drug delivery company focused on developing innovative technologies, improved medicines and life cycle management products. Kashiv also offers contract research and development services to pharmaceutical clients in need of formulation and analytical development expertise and/or clinical supply manufacture.
This is an outstanding opportunity for you to stand out and make your mark. Kashiv is looking for a dynamic Manager of Regulatory and Clinical Affairs. In this critical role and as part of Kashiv’s team, you will pro-actively develop, lead and drive the execution of regulatory strategy and systems, as well as develop a submission and clinical trial strategy for US and international countries.
You will support new product development efforts and international expansion, and ensure regulatory compliance associated with submission preparations, regulatory filings, premarket clearances, labeling, reviews, certifications etc.