Sr. Regulatory Affairs Supervisor
2 months ago
Are you motivated by driving innovation for the life-changing benefit of patients? Are you ready to help transform the treatment paradigm for a broad range of chronic diseases that currently rely on injection-based therapies? Then this is your moment. Apply now and join Novo Nordisk. Together we can create life-changing innovation. Together we can make it happen.
The position
Regulatory Planning Submissions and Approvals for new products, license renewal, variation, eregistration, etc Regional Regulatory Affairs Regulatory Compliance & System Cross Functions/Departments Supporting Regulatory InfluenceQualifications
Relevant graduate level degree, e.g. Pharmacy, Pharmacology, Biology. Fluency in both written & spoken English Min 3 year experience in pharmaceutical industry or related industry like medical devices or healthcare industry More than 1 year working experience in regulatory affairs or medical department and working experience on international pharmaceutical company is preferred Undertake the basic RA tasks independently. Team working characteristic Active & creative thinking abilityAbout the department
In CMRQ (Clinical Medical Regulatory and Quality),We commit to bringing our products to Chinese market with the fastest speed and top quality, and applying the most scientific way to communicate our products' benefits to our customers. We have 6 team in CMRQ aiming to portfolio evaluation and overall strategy; New product approval, licence maintenance, Product localization; Clinical evidence trial operation Phase (I-IV, NIS); Multiple stakeholders’ engagement (HA/KOLs/investigators) and Medical evidence generation/communication.
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(Sr.) Regulatory Affairs Specialist
4 weeks ago
Beijing, China Abbott Full timeMAJOR RESPONSIBILITIES: Responsible for registration of medical device, IVDs and/or drug products. Responsible for the applications for New Product registration, variations of marketed products and license renewals within the set timeframe and conducting in compliance with NMPA/CMDE requirements as well as relevant internal SOP. Responsible for...
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Sr. Regulatory Affairs Supervisor
2 months ago
Beijing, China Novo Nordisk Full timeAre you motivated by driving innovation for the life-changing benefit of patients? Are you ready to help transform the treatment paradigm for a broad range of chronic diseases that currently rely on injection-based therapies? Then this is your moment. Apply now and join Novo Nordisk. Together we can create life-changing innovation. Together we can...
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Regulatory Affairs Specialist
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Regulatory Affairs Manager
2 months ago
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Regulatory Affairs Manager
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Regulatory Affairs Specialist
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Regulatory Affairs Specialist
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Regulatory Affairs Specialist
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Regulatory Affairs Specialist
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Beijing, Beijing, China 1215 GlaxoSmithKline (China) Investment Co Ltd Full timeRole Overview:We are seeking a highly motivated and experienced Regulatory Affairs Specialist to join our team at GSK China. As a key member of our regulatory affairs team, you will be responsible for providing strategic and technical regulatory support to our line manager to ensure timely and high-quality submission and approval of our products in the...
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Regulatory Affairs Specialist
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Beijing, Beijing, China Novo Nordisk Full timeAre you passionate about driving innovation in the pharmaceutical industry? Do you want to contribute to the development of life-changing treatments for patients? We're seeking a highly motivated and experienced Regulatory Affairs professional to join our team at Novo Nordisk.About the RoleDevelop and implement regulatory strategies for new products and...
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Regulatory Affairs Specialist
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Regulatory Affairs Specialist
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Beijing, Beijing, China Novo Nordisk AS Full timeAre you passionate about driving innovation in the pharmaceutical industry? Do you want to make a meaningful impact on the lives of patients? We're seeking a highly motivated and experienced Regulatory Affairs professional to join our team at Novo Nordisk A/S.The RoleDevelop and implement regulatory strategies to ensure compliance with global regulations and...
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Regulatory Affairs Specialist
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Beijing, Beijing, China Novo Nordisk AS Full timeAre you passionate about driving innovation in the pharmaceutical industry? Do you want to make a meaningful impact on the lives of patients? We're seeking a highly motivated and experienced Regulatory Affairs professional to join our team at Novo Nordisk A/S.The RoleDevelop and implement regulatory strategies to ensure compliance with global regulations and...
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Regulatory Affairs Manager
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Regulatory Affairs Specialist
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