A Regulatory Affairs and Quality Assurance professional with a solid scientific background. Adept knowledge in Medical Devices, Pharmaceutical Sciences, Pre-clinical and Clinical Aspects of Drug Development, Consumer Health Care, Biochemistry, Immunology, Biotechnology. Possesses strong communication skills and ability to think analytically, as well as has a proven track record of improving the efficiency of the business processes.Specialties: Regulatory and Quality Compliance ~ Government Liaison ~ Medical Devices ~ ISO 13485:2016 ~ ISO 19011:2018 ~ MD QMS ~ Leading Management Systems Audit Teams ~ Consumer Products ~ Project Management ~ Customer Focus ~ Lean Practices ~ Data Analysis ~ Scientific Writing ~Effective Communication and Collaboration ~ Scientific Research ~Continuous Professional Growth ~ Process Management ~ Change Management ~ Leadership ~ Mentoring