Job Description : Government Affairs (GA)Manager Acting as a business enabler to proactively co-create and drive business values with regulatory resources, GA manager plays an supportive role to foster Siemens image and make Siemens a trusted and re
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Job Description At Bristol Myers Squibb, we are inspired by a single vision - transforming patients lives through science. In oncology, hematology, immunology and cardiovascular disease - and one of the most diverse and promising pipelines in the in
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1. Principal Duties and Responsibilities (General Summary, essential functions and authorities, etc.) 主工作责(基本概况,主功能,等) 法规事务专员由其直线监管。法规事务专员负责多个法规事务项目的计划执行和交付,以实现公大目标。法规事务专员负责在直线的监管下计划并执行所分项目的注册工作;负责调跨能部门之间的工作,包括研生产质医学事务临床法务
Be responsible for identifying and collecting applicable medical device regulations and standards in China, understanding the requirements of regulations, timely updating and popularizing knowledge of new regulations and policies in organization Prop
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Job Description Summary Responsible for Imported BDI_PI Products Regulatory AffairsJob Description 1. Maintain current NMPA approved certificates, including extension registration, change registration and support BU&RC to resolve post-marketing issue
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* interpret federal, state, provincial, and international regulations as they apply to Beckman Coulter products, processes and/or procedures advises on impact of regulations, and devises strategies to compliance. They may liaise with external regul
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The A2R Senior Executive is accountable for the processing of transactions related to: * Closing and reporting of financial books * Local tax reporting * Statutory compliance This role will support the A2R Team in ensuring t
DESCRIPTION Job summary We are looking for an independent, passionate, and deeply experienced professional with expertise and experience in leading the development of industry regulatory standards, translating complex financial regulatory requiremen
Gilead Sciences is continuing to hire for all open roles. Our interview process may be conducted virtually and some roles will be asked to temporarily work from home. Over the coming weeks and months, we will be implementing a phased approach to brin
The Global Regulatory Team Leader (GRTL) is part of the Global Regulatory Affairs (GRA) organization within the Sanofi Vaccines Global Business Unit. The GRTL will report to the GRA Endemics and New Technologies Franchise Head and will be responsible
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Position Description: The incumbent Clinical Specialist (Project Manager) will provide tactical and operational support for Global Product Safety & Medical Scientific Affairs, serving as a liaison for clinical & medical scientific support in Asia Pac
Job Description : JOB SUMMARY: Establish and strengthen site regulatory expertise & capability to support biological drug substance and drug product CDMO business. * Provide expertise in NMPA's IND/BLA submission pathway and regulatory requiremen
Are you interested in working for a global company where you can work across functions and on awide-varietyof projects As a member of Stryker's RA/QA team, that is exactly what you will do! Here, we provide our Regulatory Affairs team the opportunit
This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we
Job Description : Company Information About Thermo Fisher Scientific Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science. Our mission is to enable our customers to make the world healthier, cleaner and safer. With reven
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Job description As the executive leader of Global Clinical and Medical affairs , including team building,determination of responsibilities and requirements of each post, establishment of performance evaluation system, assessment of team members and p
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Are you inspired by 'what's next' So are we. When you join the Albemarle team, you contribute to a better tomorrow. You will play a role in powering many of the world's largest and most critical industries, from energy and communications to transpor
Associate, Compliance Risk and Diligence, China In a world of disruption and increasingly complex business challenges, our professionals bring truth into focus with the Kroll Lens. Our sharp analytical skills, paired with the latest technology, allow
Job Description : . Make the registration strategy and plan based on the business needs . Be responsible for the new/alteration/renewal registrations of IVD reagents and instruments independently. . Good and close communications with BU and local co