• Over Ten years’ experience in the Bio ***** Industry with multiple levels of human management roles from the development and technology transfer to the clinical-grade manufacturing of bioprocess derived products.

• Highly trained in project management; experience includes CMC & Drug Development, cGMP manufacturing facility design (according to cGMP regulations and guidelines), validation, commissioning, and operations management of a multi-product site.

• Accomplished communicator and subject matter expert on regulatory compliance and other topics, including the development of in-house training courses.