[Quảng Ngãi] Công Ty QUALTECH Tuyển Dụng Chuyên Viên Business Development & Regulatory Support Full-time 2026

COMPANY INTRODUCTION
Địa điểm: Khác - Loại hình công ty: Công ty nước ngoài - Lĩnh vực kinh doanh: Y tế, Sức Khoẻ; Tư Vấn Luật, Pháp Lý - Quy mô công ty: Vừa (50 - 249 người có BHXH) - Website: [protected info] - Fanpage: [protected info]
Qualtech is an Asia Medical Device
Consulting and Clinical Trial (CRO) Company with branch offices in China, Hong
Kong, Indonesia, Japan, Malaysia, Philippines, Singapore, Vietnam, Thailand,
Korea, USA and Germany.
We are looking for a Business
Development & Regulatory Support Executive to join our Quang Ngai
office. This position offers opportunities to develop expertise in medical
device regulations and business development through professional training and
collaboration with our global teams.
Business Development & Regulatory Support Executive
Địa điểm: Khác - Tính chất công việc: Toàn thời gian - Chuyên môn: Bán hàng (Sales) - Kinh nghiệm: Không cần kinh nghiệm - Đừng lo! Chúng tôi sẽ đào tạo bạn từ đầu. Có kinh nghiệm là điểm cộng!; Yêu cầu ứng viên có kinh nghiệm - Mức lương: Thỏa thuận
JOB DESCRIPTION
Build and maintain client
databases, focusing on global medical device manufacturers.
Support the Sales team in
handling client inquiries, preparing service quotations, and following up on
business opportunities.
Communicate with global clients
and coordinate with internal teams on business development and regulatory
matters.
Assist in preparing basic
materials for presentations or promotional use when required.
Support promotion of company
events (e.g., webinars).
Support regulatory submissions
for assigned projects/countries, which may include completion of submissions or
notifications, as required.
Learn to read and understand
regulations, technical standards, guidance documents, test reports, clinical
and medical terminology, technical product information, and complex documents.
Proactively investigate and
capitalize on regulatory information collected throughout studies and maintain
the regulatory database accordingly.
Other duties as
assigned.
REQUIREMENTS
Major in related fields, such as
Business Administration, Economics, International Business, Foreign Languages,
Biomedical Engineering, Biotechnology, or Medicinal Chemistry.
Fluent in English is a must;
other languages will be an advantage. Candidates who can speak Chinese will
be a big plus.
Fresh graduates or candidates
with 0-2 years of working experience are welcome. Prior experience in RA is not
required; professional training will be provided.
Ability to manage multiple
projects, set priorities to meet deadlines.
Keeping attention to details.
Strong interpersonal skills,
both written and oral.
Basic skills in MS Office: Word,
PowerPoint, Excel, Outlook.
Prior experience in Sales,
Business Development or Customer Service will be an advantage.
Gender: Female.
Prioritize Quang Ngai residents.
BENEFITS
Salary: negotiated
Social Insurance, Medical
Insurance, Unemployment Insurance benefits.
13th month pay (shall
consecutively work for 1 year).
Annual leave with pay.
Professional training in medical
device regulatory affairs and business development.
Professional, dynamic working
environment.
Have a chance for oversea
training.
HOW TO APPLY
Submit your application via the APPLY NOW button below.
Deadline: 23:59 30/11/2026
Note: Only selected candidates will be contacted (via email). Make sure that your email and Spam/ Promotions box are checked regularly so that you will not miss any notifications from us.
APPLY NOW