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【Job Summary】
- Responsible for managing the Regulatory Affairs Department
【Main responsibilities】
- Lead and manage the Regulatory Affairs Department, ensuring department operations comply with legal requirements and company standards.
- Ensure drug registration processes are completed on time and meet legal requirements.
- Engage in building relationships with drug regulatory agencies and related organizations.
- Develop strategies and plans to ensure efficient and expedient drug registration processes.
- Ensure compliance with procedures and quality standards related to drug registration documents.
- Provide creative and optimized solutions to enhance efficiency and competitiveness in drug registration processes for the company.
- Graduated from university with a major in pharmacy or related fields.
- At least 3 years of experience in regulatory affairs management
- Understanding of regulatory affairs procedures and regulations of drug administration.
- Knowledge of quality control procedures and legal requirements related to regulatory affairs documents.
- Pharmacy Specialized English proficiency (upper-intermediate)
- Willing to learn Japanese in the near future
【Company/Job Attraction】
- Professional and friendly work environment, opportunities for career development.
- Participation opportunities in high-quality drug registration processes.
- Opportunities for advancement within the company and involvement in significant projects.
- Training and enhancement of professional and management skills.
-13 month bonus
-Company trip
-Parking fee
-Gasoline fee
-Social insurance & medical insurance(related to Vietnamese law)
-12 days paid leave(if CDD kept belonging more than 5 years, the paid leave will increase such as 13 days)
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Công Ty TNHH Reeracoen Việt Nam
Công Ty TNHH Reeracoen Việt Nam
Công Ty TNHH Reeracoen Việt Nam
Công Ty Cổ Phần Global Optima
Công Ty TNHH NNR Global Logistics (Việt Nam)
Chi Nhánh Miền Nam - Công Ty Cổ Phần Mỹ Phẩm Quốc Tế Thùy Dung
Công Ty TNHH The Matrix
Công Ty Tài chính TNHH HD SAISON