Sr. Regulatory Affairs Supervisor

2 months ago


Beijing, China Novo Nordisk AS Full time

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 Influence

Qualifications

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 ability

About 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.



  • Beijing, China Abbott Full time

    MAJOR 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...


  • Beijing, China Novo Nordisk Full time

       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...


  • Beijing, Beijing, China 1215 GlaxoSmithKline (China) Investment Co Ltd Full time

    Job Purpose:The Head of Regulatory Affairs, China will provide strategic direction for the GSK China Regulatory Affairs team. The role will ensure the registration of new products and line extensions and manage the life cycle of the products in line with commercial and global regulatory objectives. The role will maintain strategic relationships with key...


  • Beijing, Beijing, China Novo Nordisk AS Full time

    Key ResponsibilitiesWe are seeking a highly skilled Regulatory Affairs Manager to join our team at Novo Nordisk A/S. As a key member of our regulatory team, you will be responsible for ensuring compliance with regulatory requirements and guidelines.Develop and implement regulatory strategies to support the launch and maintenance of our pharmaceutical...


  • Beijing, Beijing, China 1215 GlaxoSmithKline (China) Investment Co Ltd Full time

    Job Title: Senior Regulatory Affairs ManagerJob Summary:We are seeking a highly skilled Senior Regulatory Affairs Manager to join our team at 1215 GlaxoSmithKline (China) Investment Co Ltd. As a key member of our regulatory affairs team, you will provide strategic and technical regulatory support to our line manager to facilitate the submission and approval...


  • Beijing, Beijing, China Novo Nordisk Full time

    About the RoleWe are seeking a highly motivated and experienced Regulatory Affairs professional to join our team at Novo Nordisk. As a Regulatory Affairs Manager, you will play a key role in ensuring the compliance of our products with regulatory requirements and ensuring the smooth approval process of new products.Key ResponsibilitiesDevelop and implement...


  • Beijing, Beijing, China Novo Nordisk AS Full time

    About the RoleWe are seeking a highly motivated and experienced Regulatory Affairs professional to join our team at Novo Nordisk A/S. As a key member of our Clinical Medical Regulatory and Quality department, you will play a critical role in driving innovation and transforming the treatment paradigm for chronic diseases.Key ResponsibilitiesDevelop and...


  • Beijing, Beijing, China Novo Nordisk AS Full time

    Are you passionate about driving innovation in the pharmaceutical industry? Do you want to make a meaningful impact on the lives of patients? Novo Nordisk A/S is seeking a talented Regulatory Affairs Specialist to join our team.The PositionDevelop and implement regulatory strategies for new products and submissionsCollaborate with cross-functional teams to...


  • Beijing, Beijing, China Novo Nordisk Full time

    Key ResponsibilitiesAs a Regulatory Affairs Manager at Novo Nordisk, you will play a critical role in ensuring the company's products meet regulatory requirements and are approved for market access. Your key responsibilities will include:Developing and implementing regulatory strategies to support product launches and lifecycle management.Preparing and...


  • Beijing, Beijing, China Hologic, Inc. Full time

    Job SummaryWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Hologic, Inc. This role will be responsible for establishing and maintaining registration plans for medical devices, forecasting and managing project budgets, and coordinating submissions to regulatory agencies.Key ResponsibilitiesDevelop and execute registration...


  • Beijing, Beijing, China Novo Nordisk Full time

    Are you passionate about driving innovation in the pharmaceutical industry? Do you want to make a difference in the lives of patients? We are seeking a highly motivated and experienced Regulatory Affairs Specialist to join our team at Novo Nordisk.About the RoleDevelop and implement regulatory strategies to ensure compliance with global...


  • Beijing, Beijing, China 1215 GlaxoSmithKline (China) Investment Co Ltd Full time

    Role 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...


  • Beijing, Beijing, China Hologic, Inc. Full time

    Job SummaryWe are seeking a highly motivated and detail-oriented Regulatory Affairs Specialist to join our team at Hologic, Inc. in [Location].Key ResponsibilitiesDevelop and maintain registration plans for medical devices, ensuring compliance with regulatory requirements.Coordinate with cross-functional teams to ensure timely and accurate submissions to...


  • Beijing, Beijing, China Novo Nordisk Full time

    Are 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...


  • Beijing, Beijing, China Hologic, Inc. Full time

    Job SummaryWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Hologic, Inc. The successful candidate will be responsible for ensuring compliance with regulatory requirements and guidelines for medical device registration.Key ResponsibilitiesEstablish and maintain registration plans for medical devices, ensuring compliance with...


  • Beijing, Beijing, China Novo Nordisk AS Full time

    Are 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...


  • Beijing, Beijing, China Novo Nordisk AS Full time

    Are 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...


  • Beijing, Beijing, China 1215 GlaxoSmithKline (China) Investment Co Ltd Full time

    Job Summary:We are seeking a highly skilled Regulatory Affairs Manager to provide strategic and technical regulatory support to our line manager. The successful candidate will play a critical role in facilitating the submission and approval of our products in a timely and high-quality manner.Key Responsibilities:Provide strategic and technical regulatory...


  • Beijing, Beijing, China 1215 GlaxoSmithKline (China) Investment Co Ltd Full time

    Job Purpose:As the Head of Regulatory Affairs in China, you will provide strategic direction and leadership to the GSK China Regulatory Affairs team. Your primary focus will be on ensuring the registration of new products and line extensions, as well as managing the life cycle of products in line with commercial and global regulatory objectives.Key...


  • Beijing, Beijing, China Novo Nordisk Full time

    Are 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.The RoleDevelop and implement regulatory strategies to ensure compliance with global regulations and...