The Regulatory Affairs Specialist will be in-charge of all activities related to the licensing and registration of the company’s present and future products (medical equipment, devices, accessories, supplies and related products), and in charge of the company itself to regulatory bodies in the Philippines, including but not limited to the Department of Health (DOH) and the Food and Drug Administration (FDA). He/she shall ensure that the company complies with all legal requirements and is able to continue selling and marketing of products to all its target customers nationwide.
In the performance...