Sr. Regulatory Affairs Supervisor

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...

   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...

Are you passionate about driving innovation in the pharmaceutical industry and transforming the treatment paradigm for chronic diseases? Novo Nordisk A/S, a leading international pharmaceutical company, is seeking an experienced Regulatory Affairs Supervisor to join its team.The ideal candidate will have a strong background in regulatory planning,...

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...

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...

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...

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...

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...

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...

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...

Job DescriptionHead of Regulatory Affairs for GSK in China will provide leadership and strategic direction for the company's regulatory affairs team. The role involves ensuring the registration of new products and line extensions, managing the life cycle of products, and aligning with commercial and global regulatory objectives.About the RoleLead a team of...

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...

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...

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...

Key Responsibilities:As a Regulatory Affairs Specialist at Abbott, you will be responsible for the registration of medical devices, IVDs, and/or drug products. This includes ensuring timely submission of applications for new product registration, variations of marketed products, and license renewals, in compliance with NMPA/CMDE requirements and internal...

Job Purpose:As the Head of Regulatory Affairs, 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...

Key ResponsibilitiesDevelop and implement regulatory strategies for new products and license renewalsCollaborate with cross-functional teams to ensure regulatory compliance and system implementationSupport regulatory influence and contribute to the development of regulatory policiesQualificationsDegree in a relevant field, such as pharmacy, pharmacology, or...

Key ResponsibilitiesAs a Regulatory Affairs Manager at Novo Nordisk A/S, you will be responsible for ensuring compliance with regulatory requirements for new products, license renewals, and variations. This includes planning and executing regulatory submissions, managing regulatory systems, and collaborating with cross-functional teams.QualificationsTo be...

Job Purpose: Head of Regulatory Affairs will provide leadership and 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 stakeholder...

Job SummaryThis role requires a highly skilled and experienced professional to oversee the medical device regulatory compliance process in China. The successful candidate will be responsible for ensuring that all products meet the required regulatory standards and will work closely with the global team to achieve this goal.Key ResponsibilitiesDevelop and...