Regulatory Management Specialist

Job SummaryThe Regulatory Compliance Specialist assists with the maintenance of a portfolio of products in China, ensuring compliance with local and international regulatory requirements. This role involves preparing regulatory submissions, collaborating with internal teams, and maintaining knowledge of relevant legislation.Key ResponsibilitiesPrepare...

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...

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 DescriptionAs a Regulatory Specialist at TÜV Rheinland, you will be responsible for classifying and judging medical devices according to the MDR regulation. Your tasks will include checking the completeness of technical documents, preparing audit documents, and following up on audit projects.RequirementsTo succeed in this role, you will need a Master's...

Hologic, Inc. is seeking a highly skilled Regulatory Affairs Specialist to join our team.Job DescriptionThe ideal candidate will have more than 5 years of experience in regulatory affairs and related QA working experience in the medical device field.We are looking for someone who is familiar with imaging, surgical or IVD products and has a strong attention...

Job DescriptionWe are seeking a highly motivated and experienced Regulatory Compliance Specialist to join our team at Parexel. As a key member of our operations team, you will be responsible for ensuring the timely and accurate completion of project goals and updating applicable trial management systems.Key Responsibilities:Act as Parexel's direct contact...

About UsPfizer is a global biopharmaceutical company that applies science and our global resources to deliver innovative therapies that extend and significantly improve lives. We are committed to becoming the premier, most respected biopharmaceutical company in the world.Job SummaryWe are seeking an experienced Associate Registration Manager to join our...

Galderma offers an exciting opportunity for a highly skilled Regulatory Affairs Manager to join our team.The successful candidate will be responsible for preparing and submitting regulatory applications to obtain approval, including new products and existing license renewals and variations. This role requires strong analytical skills to monitor regulation...

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...

Transforming Patients' Lives through ScienceBristol Myers Squibb is dedicated to inspiring people to change the world. As a Regulatory Document Strategist and Manager, you will play an integral role in this mission.About UsWe are a biopharmaceutical company committed to discovering, developing, and delivering innovative treatments that address the unmet...

Key ResponsibilitiesDevelop and implement effective regulatory strategies to ensure compliance with industry regulations and standards.Lead and coordinate the submission and approval processes for new products, licenses, and variations.Establish and maintain a robust regulatory compliance system to ensure adherence to industry standards.Foster...

About the Role We are seeking a highly skilled Product Sustainability Regulatory Advisor to join our team at ExxonMobil Corporation. In this role, you will be responsible for monitoring and surveying existing and under development product sustainability (PS) regulations in the Region. You will also be responsible for understanding regulatory trends and...

About the RoleThis is an exciting opportunity for a seasoned Regulatory Affairs professional to join Pfizer's Global Regulatory Solutions (GRS) team in China. As a key member of our GRS CMC China team, you will play a crucial role in ensuring compliance with regulatory requirements and guidelines across various jurisdictions.Key ResponsibilitiesServe as a...

Transform Your Career with Bristol Myers SquibbBristol Myers Squibb is a company that transcends the ordinary. We're not just another pharmaceutical company; we're a group of innovators, researchers, and problem solvers who are passionate about transforming patients' lives through science.A Day in the Life of a Regulatory Affairs Manager - China CMCAs a...

About the RoleWe are seeking a highly skilled Regulatory Affairs Manager to join our team at Takeda in Beijing. As a key member of our regulatory affairs team, you will be responsible for ensuring compliance with drug administration and registration management regulations.Key ResponsibilitiesDevelop and implement product registration plans, coordinating with...

Job DescriptionPfizer is seeking a highly skilled Regulatory CMC Director to join our team in China. As a key member of our GRS CMC China team, you will be responsible for leading the development and execution of global regulatory strategies for projects across all aspects of drug development or manufacturing lifecycle.Main ResponsibilitiesCollaborate with...

About the RoleWe are seeking a Senior Manager CMC Regulatory Affairs Professional to join our team at 1215 GlaxoSmithKline (China) Investment Co Ltd.Job SummaryThis role is responsible for providing strategic and technical regulatory input for new and established products, ensuring timely and high-quality CMC submissions and approvals in China.Key...

Job SummaryBrenntag is seeking a highly skilled Deputy Regulatory Manager - Global Sourcing to join our team in Beijing. In this key role, you will be responsible for leading our Global Sourcing Regulatory team in ensuring compliance with all relevant laws, regulations, and industry standards.Key ResponsibilitiesCollaborate with the GSO Regulatory Manager...

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...

Your Key ResponsibilitiesAt Bayer, we strive to make a significant impact on the worldAssociate RA CMC Director Key Tasks and ResponsibilitiesRegulatory Strategy and PlanningDevelop and implement regulatory strategies for marketed chemical and bio-products, CTA, NDA in China.Timely tracking and updating project QC testing and CMC review status.Foreseeing...