Regulatory Affairs Associate

Job DescriptionCollabera is seeking a highly skilled Regulatory Affairs Associate to join our team. The ideal candidate will have a strong background in regulatory affairs, with experience in managing regulations and working with cross-functional teams.The Regulatory Affairs Associate will be responsible for:Managing regulations and working with...

Job Summary: We are seeking a highly skilled Regulatory Affairs Policy Specialist to join our team at Exelixis. The successful candidate will be responsible for gathering and interpreting global regulatory intelligence to inform Exelixis policy and practices. Key Responsibilities: Monitor the external regulatory environment to identify emerging intelligence...

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 SummaryKairos Power is seeking a highly motivated and strategic professional to lead our Government Affairs team. As a key member of our organization, you will be responsible for maintaining a daily awareness of legislative developments and policy issues impacting our priorities.This role reports to the Vice President, Regulatory Affairs & Quality, and...

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...

Abbott Laboratories is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160...

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 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,...

Actalent is a global leader in engineering and sciences services and talent solutions, driving scale, innovation, and speed to market for visionary companies. Located in a remote setting, this role is an excellent opportunity to advance your career as a Clinical Research Professional.Job Description:This Clinical Research Professional role is responsible for...

Summary: The purpose of this role is to write, or coordinate the preparation of, all clinical, regulatory and scientific documents intended to support clinical and regulatory deliverables for drug development project teams. The scope of the role includes authoring, review, and quality assurance check of documents, and management of external medical...

Summary: The purpose of this role is to write, or coordinate the preparation of, all clinical, regulatory and scientific documents intended to support clinical and regulatory deliverables for drug development project teams. The scope of the role includes authoring, review, and quality assurance check of documents, and management of external medical...

About the Opportunity:As a Post Market Surveillance Management Position, you will lead a team responsible for filing Medical Device Reports to the FDA (US), Medical Problem Reports to Health Canada, Medical Incident Reports to the EU/EFTA, and Medical Device Incident reports to the rest of the world for Abbott's division products. You will be proficient with...

SUMMARY/JOB PURPOSE: Writes and edits various documents to support Product Development. Such documents may include clinical study reports (CSRs), common technical document (CTD) summaries for submission to regulatory agencies, protocols, Investigator Brochures, literature reviews, study manuals, and standard operating procedures (SOPs). Assembles CSR and CTD...

Job DescriptionJob DescriptionPyka is looking for a Flight Operations Associate to join our experienced and enthusiastic flight operations team for the next six months with the possibility of extension. In this full time role, you will contribute to day-to-day flight test operations at our test sites across the Bay Area.The flight operations team supports...

Job Summary:The Associate Translational Medicine Director is responsible for developing and implementing translational strategies for programs in early clinical development. This role continues to support clinical programs as they progress through the pipeline, and helps to develop novel strategies to inform on dose, patient selection, and combination...

Abbott Laboratories is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160...

PRINCIPAL RESPONSIBILITIES:Under general direction of the Grievance and Appeals Leadership, the Grievance and Appeals (G&A) Coordinator II will review, investigate and process non-complex grievances for all lines of business and the completion of written communication documents to convey determination. The Coordinator is responsible for processing and...