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The Regulatory Affairs Department obtains and maintains marketing approvals of responsible products in Taiwan. It ensures full local regulatory and company compliance and provides regulatory expertise to support clinical research, product launches, and business development so as to assist in achieving business growth and full compliance with legal requirements for pharmacovigilance regarding regulatory affairs' relevant responsibilities.
The Technical Product Manager for Test & Measurement instruments will be responsible for leading the strategic planning, development, and management of our product offerings. This role requires a deep understanding of the technical aspects of test and measurement equipment, marketing plan for new product launch in Taiwan market and the ability to collaborate effectively with cross-functional teams.
This role will oversee daily operations of the production plant, ensuring onsite safety, environmental compliance, and regulatory health standards, from material intake to product delivery. They will develop and optimize processes to enhance safety, quality, and productivity throughout the facility.
管理追踪各國醫療法規與公司產品適用法規確認,ISO13485品質管理系統文件維護,並協助內外部稽核
responsible for building up the Taiwan RA foundation
As the Post-Approval Studies Manager, you'll lead our client's efforts in overseeing and driving the success of post-approval studies, ensuring compliance, high-quality data, and effective stakeholder collaboration. The role will have the opportunity to understand what's it like to post market for meds.
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