Ra/qa Manager
1 week ago
Our client is a leading medical device manufacturer in Thailand.
**Key Responsibilities**
- Interacting and coordinating with regulatory agencies to expedite the approval of registrations.
- Assisting in reviewing regulatory documents and materials such as package inserts, labels, and other packages.
- Supporting other regulatory issues such as COA translation, goods release, SOPs, etc.
- Maintaining regulatory database and reporting regularly.
- Supporting Regulatory Affairs Leader and regulatory team in preparing purchase requests, and expenditures, supporting internal communication work, meetings, sending sample testing, etc.
**Qualifications**
- Bachelor in pharmaceutical, medical technology, biosciences, or any related.
- 5 to 8 years of relevant experience in Cardiology Medical Devices Company.
- Proficient in MS Office.
- Proficient in English Communication (Spoken & Written).
- Able to work at Ayutthaya.
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