Senior Regulatory Affairs & Quality Assurance Specialist - Medical Devices
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見る: 204
更新日: 14-04-2024
場所: Ha Noi
カテゴリー: 健康/医療 製薬/化学/バイオテクノロジー
レベル: Nhân viên
給料: Cạnh tranh
教育: Đại học
経験: 3 - 6 Năm
仕事内容
JOB OVERVIEW
The Senior Regulatory Affairs & Quality Assurance Officer will be responsible for obtaining medical device pre-market regulatory approval to ensure market access is realized for product portfolio and service in the Vietnam market. Senior Officer RA/QA also will handle the sub-labeling, advertisement regulatory activities, and post-marketing regulatory activities i.e., complaint report, FSCA, Recall, etc.
Key duties & responsibilities:
- Responsible for implementing and managing the regulatory activities of medical devices in accordance with MOH registration guidelines, including new product submission, renewal submission, classification certificate, and variations submission.
- Liaise with MOH to ensure products are approved for sale as soon as possible.
- Responsible for sub-labeling, advertising, and promotion activities for regulatory compliance
- Responsible for post market surveillance activities i.e., Complaint report, FSCA, recall, etc
- Ensure product compliance for tender business.
- Responsible for database, processes, and systems to manage and maintain all regulatory documents needed for regulatory, tender application and sales
- Provide regulatory support in tender submission and corresponding inquiry as required
- Assess regulatory needs for pre- and post-marketing submission
- Input and update the global database and system as required
- Deliver the training of processes, procedures, work standards/instruction to internal and external stakeholders and ensure compliance within the delegated function
- Participate in the prediction of the effect of changes of regulations, policies, or procedure
- Coordinate with other departments i.e., supply chain, and business unit to support for product availability on the market.
- Responsible for internal and external audits such as audits from suppliers or audits to distributors.
- Assists in any ad hoc tasks as required
仕事の要件
EDUCATION AND EXPERIENCE
- A Bachelor of Science Degree with at least 3-5 years’ experience in Quality Assurance and Regulatory Affairs in MNC for Medical Devices or Pharma industry.
- Native Vietnamese speaker with fluency in English and superb communication skills in writing and speaking.
- Good working knowledge of the following software programs: Microsoft Word, Excel, PowerPoint, and Outlook.
- Proofed experience performing internal/external audits.
- Writing standard operating procedures and work instructions
仕事上の利点
- Chế độ bảo hiểm
- Du Lịch
- Phụ cấp
- Chế độ thưởng
- Chăm sóc sức khỏe
- Đào tạo
- Tăng lương
- Công tác phí
- Nghỉ phép năm
締切: 14-05-2024
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