Global Regulatory Compliance Specialist

Job Title: Global Regulatory Analyst, DemandsTesla is seeking an experienced professional to manage regulatory information requests and investigations globally.Key Responsibilities:Develop and maintain a database or tool for logging and monitoring status of all regulatory investigations and requests for information from regulators across the globe.Coordinate...

About Spectrum HealthSpectrum Health is a leading health system dedicated to delivering exceptional patient care and advancing the health of our communities. Our mission is to improve the health and well-being of the people we serve, and we are committed to providing a safe and inclusive environment for our patients, visitors, and team members.Job SummaryWe...

About Novo NordiskNovo Nordisk is a leading global healthcare company dedicated to discovering and developing innovative therapies that improve the lives of individuals with chronic conditions, particularly diabetes.Position OverviewThe Compliance Manager plays a crucial role in ensuring that all manufacturing operations adhere to applicable regulations and...

About Novo NordiskNovo Nordisk is a leading global healthcare company dedicated to the discovery and development of innovative therapies aimed at improving the lives of individuals living with diabetes. Project OverviewIn our pursuit of advancing treatment options, we are engaged in pioneering research on stem cell therapy, which holds promise for enhancing...

Regulatory Affairs SpecialistInfojini Consulting is seeking a highly skilled Regulatory Affairs Specialist to join our team. As a key member of our regulatory team, you will play a critical role in ensuring the compliance of our medical devices with EU IVD regulations.Key Responsibilities:Assist in the preparation of regulatory submissions for IVDR...

Job Title: Regulatory Affairs Associate IYoh, a Day & Zimmermann company, is seeking a highly skilled Regulatory Affairs Associate I to join our team. As a Regulatory Affairs Associate I, you will play a critical role in ensuring compliance with global regulations and cGMP requirements.Responsibilities:Assist in preparing responses to global information...

About the RoleWe are seeking a highly skilled Senior International Regulatory Product Specialist to join our Diabetes Care Division at Abbott. As a key member of our team, you will play a critical role in ensuring the efficient and compliant business processes and environment for our regulatory department.Key ResponsibilitiesAssist in the development and...

Exciting Opportunity for a Clinical Compliance Specialist at Spectrum HealthSpectrum Health is dedicated to improving the health and wellness of individuals. We believe in a comprehensive approach to healthcare and coverage, with a focus on prevention. Our team is committed to innovation and making a positive impact on the community.Job DescriptionAssist in...

Job SummaryWe are seeking a highly skilled Global Patient Safety Specialist to join our team at Bayside Solutions, Inc. As a key member of our clinical operations team, you will be responsible for leading the cross-functional management of Trial Master Files (TMFs) for clinical studies.Key ResponsibilitiesTMF Management: Serve as the lead for the...

The OpportunityAbbott is seeking a highly skilled Principal Regulatory Affairs Specialist to join our Diabetes Care Division in Alameda, CA. As a key member of our team, you will play a critical role in ensuring the regulatory compliance of our new product introductions in the US market.This is an exciting opportunity to work on breakthrough advancements in...

The OpportunityThis Senior International Regulatory Product Specialist will play a key role in the Diabetes Care Division at Abbott, working on-site at our Alameda, CA location. Our team is dedicated to helping people with diabetes manage their health with innovative products that provide accurate data for informed decisions. We're revolutionizing glucose...

Job SummaryWe are seeking a highly skilled TMF Specialist to join our team at Bayside Solutions, Inc. as a Global Patient Safety Trial Master File Specialist.Key ResponsibilitiesLead the cross-functional management of Trial Master Files (TMFs) for clinical studies, ensuring compliance with applicable regulations and guidelines.Oversee vendors to ensure...

Job Title: Associate Director/Director, Regulatory AffairsScribe Therapeutics is a molecular engineering company focused on creating best-in-class in vivo therapies that permanently treat the underlying cause of disease. Our team is dedicated to developing custom engineered enzymes and delivery modalities as part of a proprietary, evergreen CRISPR by...

Job SummaryWe are seeking a highly skilled TMF Specialist to join our team at Bayside Solutions, Inc. as a Global Patient Safety Trial Master File Specialist.This role will involve leading the cross-functional management of Trial Master Files (TMFs) for clinical studies, ensuring compliance with applicable regulations and guidelines.Key...

About the RoleWe are seeking a highly skilled Senior International Regulatory Product Specialist to join our Diabetes Care Division at Abbott. As a key member of our team, you will play a critical role in ensuring the efficient and compliant business processes and environment for our regulatory department.Key ResponsibilitiesAssist in the development and...

About the RoleGotion, Inc. is a leading innovator in next-generation electric vehicle and energy storage technologies, with a strong presence in the global market. We are seeking a highly skilled and experienced Tax Manager to join our team and lead our corporate tax function.Key ResponsibilitiesGlobal Tax Planning: Develop and implement tax planning...

About the RoleThis Senior International Regulatory Product Specialist will be part of the Diabetes Care Division at Abbott, working on-site at our Alameda, CA location. We're a leading healthcare company focused on helping people with diabetes manage their health with innovative products that provide accurate data to drive better-informed decisions.Key...

Job SummaryWe are seeking a highly skilled TMF Specialist to join our Global Patient Safety team. As a key member of our team, you will be responsible for leading the cross-functional management of Trial Master Files (TMFs) for clinical studies.Key ResponsibilitiesOversee the collection and filing of safety documentation into the eTMF platform.Collaborate...

Job OverviewAt TUV Rheinland, we pride ourselves on being a premier provider of testing, inspection, and certification services globally, employing over 20,000 dedicated professionals. Our workforce is our greatest asset, and we are committed to fostering their growth through competitive compensation, a variety of health insurance options, and a robust...

Job SummaryWe are seeking a highly skilled Global Patient Safety Specialist to join our team at Bayside Solutions, Inc. As a key member of our clinical operations team, you will be responsible for leading the cross-functional management of Trial Master Files (TMFs) for clinical studies.Key ResponsibilitiesTMF Management: Serve as the lead for the...