Across my experience in multinational environment as a regulatory affairs specialist, i have integrated regulatory knowledge throughout the healthcare product lifecycle with aspects of effective management and strategy development, and also developped basic knowledge and understanding of the regulatory and legal frameworks, regulatory requirements, processes and procedures.
I am involved in many projects, which helps me demonstrate the acquired knowledge and skills in areas such as quality assurance and audits, documentation management, risk-benefit analysis; communication and collaboration internally and externally; submission, registration, obtaining approvals, and batch release to the...