Senior Regulatory Labeling Specialist

Senior Specialist, Regulatory Affairs, Critical Care Company: Edwards Lifesciences LLC Position: Req-33420 Location: Irvine, CA Posted: May 13, 2024 Make a meaningful difference to patients around the world. From design to production, our Regulatory Affairs teams help guide our innovative technologies through complex domestic and international regulatory...

Job Description Job Description Salary: $100k + DOE OrthAlign, Inc. , a Smart Technology, growing medical device company, has an immediate opening for a Senior Regulatory Affairs Specialist responsible for implementing regulatory strategies, assisting with the preparation, organization, and maintenance of documentation sufficient to ensure regulatory...

Job DescriptionJob DescriptionSalary: $100k + DOEOrthAlign, Inc., a Smart Technology, growing medical device company, has an immediate opening for a Senior Regulatory Affairs Specialist responsible for implementing regulatory strategies, assisting with the preparation, organization, and maintenance of documentation sufficient to ensure regulatory compliance...

Position: Senior Regulatory Affairs Specialist Employment type: 1 year Contract/ Permanent Location: Jacksonville, FL or Irvine CA - 2 days per week ClinChoice is a global CRO that offers high-quality one-stop service to biopharmaceutical, medical device, and consumer products clients. Some of these services include clinical operations, project management,...

Role: Sr Regulatory Affairs SpecLocation: Irvine, CA - 92606Duration: 9 MonthsJob Description• Create regulatory submissions (exercising judgment to protect proprietary information) for finalization and submission by OUS EW affiliates; track timelines and document milestone achievements, participate in developing regulatory strategy, prioritize submissions...

Position: Senior Regulatory Affairs SpecialistEmployment type: 1 year Contract/ PermanentLocation: Jacksonville, FL or Irvine CA (ONSITE 2 days per week - HYBRID ROLE)ClinChoice is a global CRO that offers high-quality one-stop service to biopharmaceutical, medical device, and consumer products clients. Some of these services include clinical operations,...

????????????????: Sr Regulatory Affairs Spec ????????????????????????????????: Irvine, CA Duration: 09 Months Must be able to speak Japanese Job Description: Summary: The main function of a regulatory affairs specialist is to complete and maintain regulatory approvals and clearances of assigned products. Key Responsibilities: Create regulatory submissions...

𝐑𝐨𝐥𝐞: Sr Regulatory Affairs Spec𝐋𝐨𝐜𝐚𝐭𝐢𝐨𝐧: Irvine, CADuration: 09 MonthsMust be able to speak JapaneseJob Description:Summary:The main function of a regulatory affairs specialist is to complete and maintain regulatory approvals and clearances of assigned products.Key Responsibilities:Create regulatory submissions...

: Sr Regulatory Affairs Spec : Irvine, CADuration: 09 MonthsMust be able to speak JapaneseJob Description:Summary:The main function of a regulatory affairs specialist is to complete and maintain regulatory approvals and clearances of assigned products.Key Responsibilities:Create regulatory submissions (exercising judgment to protect proprietary information)...

: Sr Regulatory Affairs Spec : Irvine, CADuration: 09 MonthsMust be able to speak JapaneseJob Description:Summary:The main function of a regulatory affairs specialist is to complete and maintain regulatory approvals and clearances of assigned products.Key Responsibilities:Create regulatory submissions (exercising judgment to protect proprietary information)...

We are NeuroVasc Technologies! We are committed to being the most dynamic creator of neurovascular devices in the world. We deliver excellence through innovation with integrity. Reporting directly to the CEO, the Senior Regulatory Specialist is responsible to plan, direct and coordinate global product registrations and lead regulatory submissions planning...

Overview: MedAlliance is a leading and innovative combination medical device company dedicated to improving patient outcomes and enhancing healthcare worldwide. We specialize in the development, manufacturing, and commercialization of cutting-edge coronary and peripheral medical devices that integrate pharmaceuticals with traditional medical devices. Our...

We are NeuroVasc Technologies! We deliver excellence through innovation with integrity.Reporting directly to the CEO, the Senior Regulatory Specialist is responsible to plan, direct and coordinate global product registrations and lead regulatory submissions planning and execution; collaborate with Product Regulatory and Regional Regulatory Affairs colleagues...

We are NeuroVasc Technologies! We deliver excellence through innovation with integrity. Reporting directly to the CEO, the Senior Regulatory Specialist is responsible to plan, direct and coordinate global product registrations and lead regulatory submissions planning and execution; collaborate with Product Regulatory and Regional Regulatory Affairs...

We are NeuroVasc Technologies! We deliver excellence through innovation with integrity.Reporting directly to the CEO, the Senior Regulatory Specialist is responsible to plan, direct and coordinate global product registrations and lead regulatory submissions planning and execution; collaborate with Product Regulatory and Regional Regulatory Affairs colleagues...

We are NeuroVasc Technologies! We deliver excellence through innovation with integrity.Reporting directly to the CEO, the Senior Regulatory Specialist is responsible to plan, direct and coordinate global product registrations and lead regulatory submissions planning and execution; collaborate with Product Regulatory and Regional Regulatory Affairs colleagues...

We are NeuroVasc Technologies! We deliver excellence through innovation with integrity.Reporting directly to the CEO, the Senior Regulatory Specialist is responsible to plan, direct and coordinate global product registrations and lead regulatory submissions planning and execution; collaborate with Product Regulatory and Regional Regulatory Affairs colleagues...

Summary:The main function of a regulatory affairs specialist is to complete and maintain regulatory approvals and clearances of assigned products.Key Responsibilities:• Create regulatory submissions (exercising judgment to protect proprietary information) for finalization and submission by OUS EW affiliates; track timelines and document milestone...

Summary:The main function of a regulatory affairs specialist is to complete and maintain regulatory approvals and clearances of assigned products.Key Responsibilities:• Create regulatory submissions (exercising judgment to protect proprietary information) for finalization and submission by OUS EW affiliates; track timelines and document milestone...

We are NeuroVasc Technologies! We are committed to being the most dynamic creator of neurovascular devices in the world. We deliver excellence through innovation with integrity.Reporting directly to the CEO, the Senior Regulatory Specialist is responsible to plan, direct and coordinate global product registrations and lead regulatory submissions planning and...