Government affairs jobs in Irvine, CA

 ...Status: Non-Exempt Salary: $23.00 - $27.00 per hour commensurate with skills and experience Reports to : Legislative & Government Affairs Manager Requirements: Access to reliable transportation to travel throughout the Sacramento area. Generous Benefits:... 

About the Role The role of Associate Director, Medical Affairs reports to our Director of Medical Affairs and leads the review of non...  ...working with third party vendors, contracts, compliance, and governance boards. A Few Other Details Worth Mentioning: * The position... 

 ...Job Opening ID: 65652 Reports To: Director of Student Affairs Working Title: Student Affairs Assistant Department: ICS/Student Affairs/UG Bargaining Unit: CX FLSA: Non-Exempt Payroll Job Code: 004722 Job Location: UCI Campus- Irvine Percent of Time... 

 ...Regulatory Affairs Specialist Career Opportunity Job Title Regulatory Affairs Specialist FLSA Salaried Exempt Department Regulatory Reports To Director of Regulatory Affairs/ Chief Operating Officer Download the job description To apply, e-mail your resume to This email... 

 ...Overview: Join Applied Medical and play a crucial role in revolutionizing medical devices. As a Specialist in Premarket Regulatory Affairs, you will play a pivotal role in ensuring compliance with regulatory requirements during the early stages of product development.... 

 ...Job Opening ID: 67886 Reports To: Director of Clinical Research Operations Working Title: SENIOR REGULATORY AFFAIRS COORDINATOR Department: UCI Ctr for Clinical Research Bargaining Unit: RX FLSA: Exempt Payroll Job Code: 007888 Job Location: UCI Campus... 

 ...The Regulatory Affairs Specialist temp is responsible for developing and influencing regulatory policy and determining and pursuing courses of action necessary to obtain regulatory approval for the organization s products. Work with RA Leadership and Regulatory Affairs... 

 ...Education and Experience: Bachelor's degree in related field preferred. Minimum five (5) years of experience in Regulatory Affairs. Knowledge and Abilities: Proficient knowledge of general office procedures. Proficient skills in the MS Office Suite (Excel... 

 ...Description The Sr. Regulatory Affairs Specialist works under minimal supervision supporting cross- functional teams with regulatory strategy and execution for new devices and device modifications. Responsibilities Participate as the regulatory representative... 

Overview: Represents the Regulatory Affairs function in project teams, and manages regulatory projects to established timelines and budgets. Oversees and ensures compliance with state, federal and International medical device regulations and overall regulatory departmental... 

 ...Job Title Sr. Regulatory Affairs Specialist-CT/AMI Job Description The Senior RA Specialist will play a critical role in ensuring...  ...regulatory requirements for medical devices and external government product audits by China, Korea, Japan, and other inspection... 

 ...overseeing and coordinating all on-campus SGA events (election bashes, town halls, etc), planning the yearly Executive Council retreat, onboarding support staff to the organization, recording Operations, Director, Government, Student, Operation, Manufacturing, Education... 

Overview: The Director, Regulatory Affairs for EMEA is responsible for successful completion of complex regulatory projects, including pre-submissions and IDE submissions to FDA, IRB submissions, Ethics Committee submissions, EU Annex XIV submissions and as well as premarket... 

 .... For more information, visit Follow Allergan Aesthetics on LinkedIn. Job Description Description The Manager Regulatory Affairs represents US regulatory affairs for device development projects. Executes US regulatory strategic plans and provides guidance to Global... 

Support the EU's In Vitro Diagnosic Regulation (IVDR) transition activities that will impact all Bio-Rad products currenlty CE Marked under the IVD Directive. Activites include preparationrevision of technical files when needed, update labeling to comply with IVDR requirements...

 ...and securing applications on Salesforce? We are seeking an experienced Salesforce Developer to join our team to lead security & governance strategy in a multi-org environment. You will ensure that solutions deployed have technical integrity, stability, and are scalable... 

 ...Job Title Principal Regulatory Affairs Specialist Job Description Principal Regulatory Affairs Specialist (U.S. Hub based) Clinical Integration and Insight (CII) is changing the way healthcare is delivered at the point of care. Our Capsule Surveillance product... 

510(k) Premarket Notification, PMA, PMA Supplements, PMA Annual Reports, Design Dossier, Technical Files, Australian Technical Files, Canadian Licenses, and Japan submissions. Essential Requirements Checklists, Design Dossiers, Technical Files and De Regulatory, Remote,...

 .... Job Description Purpose: The Scientific Director, Medical Affairs provides specialist medical and scientific strategic and operational...  ..., data analysis and interpretation, regulatory requirements governing clinical trials and experience in development strategy and the... 

 ...direct supervision, trains with staff in the areas of Public Affairs and will have the opportunity to gain exposure to a wide range...  ...professional and technical staff with a variety of tasks such as government and media relations, community outreach and education programs...