Quality Assurance / Regulatory Affairs Executive

Responsibilities

• Responsible for all communications with the Health Authorities on products registration and related activities.

• Participates in pCm and Trademark registration

• Responsible for document (SOP, Specification, etc) preparation and review

• Involves trade team on various subjects, including export and labeling requirements, premarket regulatory requirements, and clinical study compliance issues.

• Review the packaging and marketing materials for our products to ensure the compliance Laws and Regulations.

Requirements

• Bachelor's degree in Chemistry, Biology, Biochemistry or Medical related discipline.

• Minimum 2 years experiences in QA and Regulatory affairs of Pharmaceutical/ healthcare products.

• Experience in Chinese Medicine is preferable.

• Excellent communication skills in both spoken and written English and Mandarin.

• Well organized, proven ability to work effectively to meet deadlines, proactive, proficiency in problem solving as well as good interpersonal skill

We offer competitive salary and good opportunity to the right candidate.

(All personal data collected will be used for recruitment purpose only and will be treated in accordance with our Personal Data Policy, which is available immediately upon request. Our Company reserves the right to modify the terms and conditions of package offered.)