Regulatory Affairs Lead

Job Title: Regulatory Affairs ExpertWe are seeking a highly skilled Regulatory Affairs Expert to join our team. As a key member of our regulatory affairs group, you will play a critical role in ensuring that our medical devices comply with all relevant regulations and standards.About the RoleThis is an exciting opportunity to work with a leading medical...

Job OverviewRegulatory Affairs professional sought to lead CMC regulatory support for assigned programs.Key responsibilities include formulating strategic CMC regulatory plans, collaborating with cross-functional teams, and managing the preparation of regulatory submission documents.Requirements include 8+ years of experience in Regulatory Affairs CMC, a...

OverviewOur client is a leading Rare Disease biopharmaceutical company committed to advancing innovative treatments to improve patient outcomes. Their mission is to transform care by delivering cutting-edge therapies while fostering strong scientific engagement with healthcare professionals and researchers.Our client is seeking a highly experienced Director...

Regulatory Affairs Global CMC ManagerWe are seeking a skilled Regulatory Affairs professional to lead our global CMC regulatory strategy and ensure compliance with external requirements and internal quality procedures.Develop and execute robust regulatory strategies to mitigate risks and address technical and scientific challenges.Prepare and deliver...

Regulatory Affairs ProfessionalThe ideal candidate will have a strong background in regulatory affairs, specifically in medical devices.Main Responsibilities:Develop and implement regulatory strategies to ensure compliance with European and US regulations.Support the creation and maintenance of product design and technical documentation in accordance with...

Job Overview:We are seeking a seasoned Regulatory Affairs professional to lead regulatory support for assigned programs, ensuring sound planning and tactical implementation of US and international regulatory submission strategies.The ideal candidate will have expertise in CMC regulatory strategies, strong collaboration skills, and experience serving as...

Regulatory Affairs Specialist Job DescriptionThis is a key role in our organization, responsible for post-market activities for Administration and Safety System medical devices. We are seeking an experienced Regulatory Affairs Specialist to join our team.Job Summary:The successful candidate will be responsible for performing post-market surveillance...

Job Title: Regulatory Affairs SpecialistDescription:The Senior Specialist, Regulatory Affairs position is responsible for overseeing post-market activities for medical devices and supporting departmental regulatory processes and procedures. This role also involves mentoring team members to ensure seamless execution of tasks.Key Responsibilities:Develop and...

Regulatory Affairs Professional Role OverviewThis is a key role in the development of cutting-edge structural heart devices, working closely with cross-functional teams to ensure compliance with internal and external regulatory requirements.Key Responsibilities:Clinical:Coordinate and support global clinical trial execution, including site activation,...

Job Title: Global Regulatory Affairs ManagerJob DescriptionThe role of the Global Regulatory Affairs Manager is to develop and implement regulatory strategies that ensure compliance with global regulations. This involves staying up-to-date with changing regulatory requirements, assessing risks, and making informed decisions to mitigate these...