QUALIFICATION REQUIREMENTS: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals ...
杰美特jMedtech 医疗器械 不需要融资 职位关闭 质量工程师 PQE - K· 薪 安费诺 电子/硬件开发 职位详情 厦门 3-5年 本科 8D报告 ISO13485 ISO16949 工作地址:海沧区后祥路71号协同创新园12号楼 岗位职责: 1.产品质量策划kanzhun,出具控制计划、SIP等品质文件; 2.生产异常问题追踪处理&产品良率提升; 3.检...
Recent SEC and FDA cyber regulations highlight the opportunities for medtech companies to demonstrate their commitments to safety and trust.
The new director of the FDA’s device center contrasted a European rule with the lack of mandatory reporting requirements for potential device shortages in the U.S. ByNick Paul Taylor•Jan. 17, 2025 Access now➔ Trendline Medical device industry continues to turn to AI ...
Company:SPACE (MedTech) Pte. Ltd. Designation:Software and Apps Development Intern Profession:Engineering Industry:Healthcare / Fitness / Sports Location:BedokDiscuss this Job: You can discuss this job on Clublance.com #career-jobs channel, or chat with other community members for free:Share...
The Potential for GenAI in medtech was described in “Medtech’s Generative AI Opportunity.” The remaining Ps will be covered in detail in three upcoming BCG publications. The opportunity for better outcomes, increased efficiency, and greater value creation makes GenAI the new medtech imperative....
“copilots” for workers in HR, IT, finance, and legal roles. Companies are beginning to explore the impact of gen AI on commercial and operational roles. Because of regulatory requirements, the deep integration of AI in medical products and services remains years away. However, some compa...
Johnson described the medtech industry as a “high-impact, essential” one, “not just for patients but also for economic wellbeing. Our job as a trade association is to ask these questions and bring people together.” MassMEDIC launched a working group, which Johnson said at the time would...
Streamline patient care with our advanced Patient Management System Software in NZ. Medtech Global offers efficient solutions for healthcare professionals.
The MedTech industry is undergoing extensive changes with the advent of theEuropean Union Medical Device Regulation(EU-MDR) framework, a comprehensive set of regulations being implemented across Europe. It establishes more stringent requirements to mitigate the negative impact of hazardous substances in ...