Our client is a medical devices company.
Job Responsibilities
- Analyze and oversee the requirements for product registration in the local market, collaborating closely with the global organization and the regional quality manager to secure all necessary local product approvals and registrations.
- Identify and execute strategies to minimize costs and reduce the time required to launch new or updated products.
- Attend meetings with local authorities and technical committees, anticipating and adapting to changes in regulatory rules affecting the business.
- Develop and manage integrated management systems and certifications for sales and service entities within the country.
- Implement and manage quality-related tasks and procedures, addressing any quality issues to meet set quality targets.
Requirements
- More than 10 years of regulatory affairs experience in the medical devices industries
- Good command of spoken and written Thai and English
If you are interested, please submit your CV by clicking the 'APPLY' or send it to pacita.phaohusara@jac-recruitment.com
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