Mô tả công việc
- Conduct independent evaluation, selection, and application in making adaptations and modifications to products and processes.
- Manage and provide leadership for the functional group’s development, direction, and effectiveness, adhering to organizational policies and processes and supporting overall business and corporate objectives.
- Implement and understand FDA or regulatory requirements as necessary.
- Apply technology principles to multiple tasks. Working knowledge of cross-functional and related technical areas.
- Highlight risks and understand how to approach and complete tasks, avoiding serious delays and considerable expenditure of time and resources.
- Follow technical specification requirements and provides feedback on various technical processes and procedures.
- Present effectively complex technical information/analysis, and respond to questions from technical staff members and management.
Yêu cầu công việc
- More than 2 years experience in development, production, quality assurance, regulatory affairs or quality management of medical devices
- Willingness to travel business trips
- Experience in auditing is a plus
- Problem solving skill & customer service mindset
Quyền lợi được hưởng
- Working from Mon- Fri
- Attractive salary package