Jobs
>
Irvine

    Regulatory Affairs Specialist - Irvine, United States - Trinus

    Default job background
    Description

    Job Description

    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 (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 with operating plans as well as ensuring alignment with KOD in countries (e.g., OUS, [the globe minus US, EU, Canada]).

    Participate in providing guidance on strategies and contingency planning with respect to OUS regulatory requirements, including assessing impact of proposed and current global regulations and proposing suggestions for expediting approvals.

    Participate in representing the OUS regulatory function on manufacturing and product development teams to provide input on regulatory requirements, including presenting alternatives for meeting regulatory requirements and resolving conflicts between those requirements and development issues, and/or reporting to management.

    Participate in providing guidance and feedback to business unit regulatory teams on registration requirements for new and renewal registrations, product and process changes, and review of labeling content? and guidance on process improvement projects, based on prior experience and responses from affiliates.

    Other incidental duties assigned by Leadership.

    Education and Experience:

    Bachelor's Degree or equivalent in scientific discipline (e.g., Biology, Microbiology, Chemistry)
    5-7 years of experience required

    Trinus Corporation, a leading provider of technology solutions and services with over 25 years of experience, is a certified WBE/MBE/SBE/SDB firm accredited by WBENC, NMSDC, and SBA.


    Our mission is to shape the future of work by aligning the right mix of people, process, technology, and innovation to efficiently meet our clients' business objectives.

    At Trinus, we understand that finding the right opportunity is pivotal in your career journey. Our staffing services go beyond mere placements; they are about matching your skills and aspirations with the perfect fit.

    To learn more about us, please visit our website


  • Jenavalve Technology Inc Irvine, United States

    **Job Title**: Specialist, Clinical Affairs · **Supervisor/Manager Title**:Senior** **Manager, Clinical Affairs · **Job Description Summary**:Supports Clinical Research Associates (CRAs) to manage specific activities related to clinical projects. · **Responsibilities**: · - Provi ...


  • Edwards Lifesciences Irvine, United States

    Make a meaningful difference to patients around the world. From design to production, our Regulatory Affairs teams help guide our innovative technologies through complex international regulatory environments. Working in partnership with external government and regulatory authorit ...


  • Cordis Irvine, United States

    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 medica ...


  • Nihon Kohden Irvine, United States

    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 other members of the RA team ...


  • Orange County Sanitation District Fountain Valley, United States

    **Description**: · - What do **you **value in your next job? · At the **Orange County Sanitation District **our **Core Values **form the framework of our organization and reinforce our professional work ethic. If the following values ring true with you, we'd love to invite you to ...


  • Medtronic Santa Ana, United States

    **Associate Regulatory Affairs Specialist (hybrid)** · Cardiac surgery represents end-state treatment in the care continuum for many cardiovascular diseases. There are approximately 1.8 million cardiac surgical procedures in the world on an annual basis. Cardiac surgery remains e ...


  • Kelly Services, Inc. Irvine, United States

    The Regulatory Affairs Specialist II, will provide administrative and technical support to regulatory affairs leadership in order to facilitate compliance with U.S. and international regulatory requirements. The Regulatory Affairs Specialist provides Regulatory Affairs, Specialis ...


  • Kelly Science, Engineering, Technology & Telecom Irvine, United States

    Regulatory Affairs Specialist (hybrid) · Kelly Science and Clinical FSP is currently seeking a medical device Regulatory Affairs Specialist II for a long-term engagement in Irvine, CA with one of our Global Pharmaceutical clients. This person will join our Kelly FSP (Functional S ...


  • Tucker Parker Smith Group (TPS Group) Irvine, United States

    Job Title: Regulatory Affairs Specialist · Location: Irvine, CA · Schedule: Hybrid, Monday to Friday, 8 AM to 5 PM, with on-site work Tue/Thur · Duration: 1 year with potential to extend/ convert to internal FTE · no fully remote option · hourly rate of $40-45/hr · About Us: We a ...


  • Kelly Science, Engineering, Technology & Telecom Irvine, United States

    The Regulatory Affairs Specialist III, will provide administrative and technical support to regulatory affairs leadership in order to facilitate compliance with U.S. and international regulatory requirements. The Regulatory Affairs Specialist provides direct Worldwide Regulatory ...


  • Kelly Science, Engineering, Technology & Telecom Irvine, United States

    The Regulatory Affairs Specialist III, will provide administrative and technical support to regulatory affairs leadership in order to facilitate compliance with U.S. and international regulatory requirements. The Regulatory Affairs Specialist provides direct Worldwide Regulatory ...


  • Kelly Science, Engineering, Technology & Telecom Irvine, United States

    Regulatory Affairs Specialist (hybrid) · Kelly Science and Clinical FSP is currently seeking a medical device Regulatory Affairs Specialist II for a long-term engagement in Irvine, CA with one of our Global Pharmaceutical clients. This person will join our Kelly FSP (Functional ...


  • Kelly Science Engineering Technology & Telecom Irvine, United States

    Regulatory Affairs Specialist (hybrid) · Kelly Science and Clinical FSP is currently seeking a medical device Regulatory Affairs Specialist II for a long-term engagement in Irvine, CA with one of our Global Pharmaceutical clients. This person will join our Kelly FSP (Functional ...


  • Edwards Lifesciences Irvine, United States

    Make a meaningful difference to patients around the world. From design to production, our Regulatory Affairs teams help guide our innovative technologies through complex international regulatory environments. Working in partnership with external government and regulatory authorit ...


  • MyKelly Irvine, United States Full time

    Regulatory Affairs Specialist · The Regulatory Affairs Specialist II, will provide administrative and technical support to regulatory affairs leadership in order to facilitate compliance with U.S. and international regulatory requirements. The Regulatory Affairs Specialist provid ...


  • Brett Fisher Group Irvine, United States

    Job Description · Job DescriptionThis is a rare opportunity to join the global regulatory team of an innovative, fast-paced, medical device company. The Company values intellectual curiosity, self-starters with a willingness to grow and expand their impact on the organization, em ...


  • Brett Fisher Group - Search Consultants Irvine, United States

    This is a rare opportunity to join the global regulatory team of an innovative, fast-paced, medical device company. The Company values intellectual curiosity, self-starters with a willingness to grow and expand their impact on the organization, employees who find meaning in worki ...


  • University Of California Irvine Irvine, United States

    · Job Opening ID: 69779 Reports To: Director of Graduate Studies Working Title: GRADUATE AFFAIRS SPECIALIST Department: SOM-Graduate Studies Bargaining Unit: 99 FLSA: Exempt Payroll Job Code: Job Location: UCI Campus- Irvine Percent of Time: 100% Work Schedule: 8-5, M-F Employee ...


  • Compunnel Irvine, United States

    Job Description: 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 final ...


  • Ledgent Technology Irvine, United States

    · 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 finaliza ...