Regulatory Affairs Specialist

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...

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...

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...

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...

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...

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 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...

Key ResponsibilitiesAs a Regulatory Affairs Specialist at Novo Nordisk, you will be responsible for planning and executing regulatory strategies to ensure compliance with global regulations. This includes submissions and approvals for new products, license renewals, variations, and deregistrations.QualificationsRelevant graduate-level degree in a field such...

Job Summary:Abbott is seeking a highly skilled Regulatory Affairs Specialist to join our team. As a key member of our regulatory team, you will be responsible for ensuring compliance with regulatory requirements for medical devices, IVDs, and drug products.Key Responsibilities:Registration of medical devices, IVDs, and/or drug productsApplications for New...

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...

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...

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...

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...

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 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...

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

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...

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...

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...