Regulatory Affairs Specialist

AliveCor seeks a Senior Regulatory Affairs Specialist to join this exciting start-up that is changing the face of mobile health. In this role, you will be part of the regulatory team responsible for proper oversight of medical device development and market introduction. You will work closely with Quality, Engineering, Product Management, Marketing and...

DescriptionAt AliveCor, we imagine a healthier world powered by access to personalized intelligent information. Heart disease kills more people than anything else in the western world, including all cancers combined. We're on a mission to be the worlds heart health partner by enabling access to quality heart care for everyone. AliveCor has pioneered...

Job TitleRegulatory Affairs SpecialistJob DescriptionJob Title : Regulatory Affairs SpecialistJob Responsibilities:• Monitors global regulatory changes, interprets requirements, and integrates findings into regulatory strategies, ensuring timely communication with teams.• Implements regulatory strategies for international markets, collaborating with...

Job TitleRegulatory Affairs SpecialistJob DescriptionMinimum required Education: High School Diploma, Vocational Education / Bachelor's Degree in Business Administration, Communications, Quality Management, Biomedical Engineering, Business Administration, Health Sciences, Pharmaceutical, Law or equivalent. Minimum required Experience: Minimum 2 years of...

Job Title: Regulatory Affairs ManagerDepartment: Regulatory Affairs / Quality & ComplianceReporting to: Head Regulatory AffairsJob Purpose:To lead and oversee all regulatory affairs activities, ensuring company products comply with applicable local and international regulatory requirements. The role involves developing regulatory strategies, managing...

Job Description SummaryJoin GE HealthCare as a Lead Specialist in Regulatory Affairs and play a pivotal role in shaping the future of medical imaging. This global leadership position offers the opportunity to drive regulatory strategies and lead cross-functional teams to bring innovative X-ray imaging products to market. Be part of a dynamic environment...

Job TitleRegulatory Affairs Operations SpecialistJob DescriptionJob Responsibilities:International RegistrationsUpload, Verify, and Validate the data with new Regulatory Information to the RIM databaseMaintain Registration &Licensing InformationCreate Submission Packages for International RegistrationsInitiate Renewals with the countries.Initiate Product...

Company DescriptionSilmed Scientific is a global leader in regulatory affairs, specializing in delivering comprehensive end-to-end regulatory solutions for pharmaceuticals, medical devices, and biosimilars. With expertise in regulatory strategy and successful drug development, the company supports approvals across global markets including Europe, the US,...

OverviewTheRegulatory Affairs Specialist IIhas primary responsibility for provision ofIn Vitro Diagnosticregulatory support to p repare, execute and maintain regulatory filings including change management, support of post market requirements and support of outside vendors [e.g. license holders, in country representatives].Secondary responsibility would be to...

Company Profile:At Sea6 Energy we envision a future where we can harness the potential of the oceans – to provide sustainable solutions in energy, agriculture and food. To accomplish this, a multidisciplinary team with professionals from diverse fields of science including Industrial automation, Biotechnology, Agriculture, Ocean Engineering, Bioprocess...