Company Description
Vee Care (Asia) Limited is a global medical device consulting firm specializing in device registration, technical documetation, quality system, compliance and market access solution.
Our Customers
Our customer include Apple, Merit, Masimo, Echnous, Lowenstein, Penumbra, MMI, IBA and Panoptics …etc
Role Descriptions
Vee Care (Asia) Limited is seeking an experienced regulatory professional to join our Taiwan regulatory consulting team as a full-time supervisory-level employee.
Your primary responsibilities will include developing regulatory dossier for TFDA and US 510k submission. This on-site role is located in Taipei City.
This position will lead a team of 2-3 members.
Qualifications
- Must
have a Bachelor's or higher degree in Science or Engineering discipline. - 3-5 years of proven experience in product design or regulatory affairs within the medical device industry, with supervisory experience considered a plus.
- Fresh graduate is also welcome for the trainee position.
- Ability to read and analyze technical reports and documents
- Strong project management, communication and collaboration skills
- Excellent verbal and written communication skills in English and Chinese
- Proven ability to work under pressure, prioritize tasks, and meet deadlines