APAC Submission Specialist

Job Tittle: Regulatory Specialist IILocation: Alameda, CA 94502 (Onsite)Rate: $59.00/hr. on w2Duration: 1 year with the possibility of extensionsShift Time: 8:00 AM to 5:00 PMNote:1 year contract and it will renewed year by year.Regulatory Submission experience not just preparing , also submitting.Writing submission of any of the APAC countries like Japan,...

Job Tittle: Regulatory Specialist IILocation: Alameda, CA 94502 (Onsite)Rate: $59.00/hr. on w2Duration: 1 year with the possibility of extensionsShift Time: 8:00 AM to 5:00 PMNote:1 year contract and it will renewed year by year.Regulatory Submission experience not just preparing , also submitting.Writing submission of any of the APAC countries like Japan,...

Job DescriptionJob Description·         Education: Bachelor’s degree·         Experience Background (Any): APAC regulatory submissions in Medical Devices or Pharmaceutical industries. Job Description (Expectation):·         Responsible for regulatory activities, including product registrations, regulatory impact assessment,...

Title: Regulatory Specialist IIDuration: 1 year with the possibility of extensionLocation: Alameda CA 94502Experience Background (Any): APAC regulatory submissions in Medical Devices or Pharmaceutical industries.Experience: 2-5 years regulatory experience and/or 2 years relevant industrial experience typically with a quality, product-development/support, or...

614462Our client, a leading Medical Device company in Alameda, CA, is looking for a Regulatory Affairs Specialist II to provides consultation/advice to regulatory specialist for change control and product development.Required Skills:2-5 years regulatory experience and/or 2 years relevant industrial experience typically with a quality,...

Details for the position are as follows:12 month contract to start with the strong possibility of extension or conversion depending on performance. Rate: $66-71 an hour. Fully onsite in Alameda, CA (open to candidates willing to relocate at their own expense. Job Description:Lead and support regulatory activities, including product registrations, impact...

The Opportunity The Principal RA Specialist – US New Product Introduction will work on-site out of our Alameda, CA location in the Diabetes Care Division. We’re focused on helping people with diabetes manage their health with life-changing products that provide accurate data to drive better-informed decisions. We’re revolutionizing the way...

Job DescriptionJob Description·         List 3-5 hard requirements for the role: Responsible for regulatory activities, including product registrations, impact assessment, etc.·         Understand country-specific requirements and deliver those to internal stakeholders, including product management, engineering, labeling, etc., for product...