- Herbalife (Torrance, CA)
- Director , Global Regulatory Affairs - Corporate Category: Legal Position Type: Regular Full-Time External ID: 14913 Location: Torrance, CA, United States ... to linkedin Apply Now **Overview** **THE ROLE:** Reporting to the VP of Global Regulatory & Post-market Safety Affairs , this individual will be responsible… more
- AbbVie (Irvine, CA)
- …you will be added to our talent pipeline and considered for future opportunities. The Director Regulatory Affairs Global Regulatory Lead, ... offices, or North Chicago, IL offices. + Responsible for leading the Global Regulatory Product Team (GRPT), developing, and implementing global strategies to… more
- AbbVie (Irvine, CA)
- …Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description The Director Regulatory Affairs , Strategic Labeling is responsible for ... and product labeling (CCDS, US/EU labeling documents) at Senior level meetings ( Global Regulatory Forum (GRF), Executive Labeling Committee (ELC), Steering… more
- AbbVie (Irvine, CA)
- … and Medical Affairs Quality Standards is responsible for the management of a RDQA global Safety, Regulatory Affairs (RA) and Medical Affairs (MA) QA ... including but not limited to Pharmacovigilance and Patient Safety, Regulatory Affairs and Medical Affairs ...regulatory requirements. Proactively monitor and interpret the external global regulatory environment for regulatory … more
- J&J Family of Companies (Irvine, CA)
- Sr Director , Regulatory Affairs Neurovascular...+ Partner with the Policy team to monitor the global regulatory landscape, assessing the impact of ... - 2406220794W **Description** **Johnson&Johnson is looking for:** **Senior Director , Regulatory Affairs , Neurovascular** **Primary Location: Galway,… more
- AbbVie (Irvine, CA)
- …Know The Associate Director / Director , Global Body Contouring, Global Aesthetics Medical Affairs (GAMA) is a key strategic leader in the GAMA ... organization. Working under the leadership of the Executive Medical Director , Global Body Contouring, GAMA in partnership with key medical functional teams; the… more
- AbbVie (Irvine, CA)
- …for a product(s) within a Therapeutic Area and supports the Manager (Senior Manager, Associate Director , Director ( Global Regulatory Lead (GRL)), in the ... YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Manager, Global Regulatory Strategy US & Canada is responsible for the… more
- AbbVie (Irvine, CA)
- …Marketing and Sales- Director - Strategic Accounts and their leadership. + Regulatory Affairs ; Legal; OEC. + US Medical Information; Pharmacovigilance. + ... environment, by creating trust and respect with the Medical Affairs field leadership as well as Director (s)-Strategic...the US Area Head- Global Aesthetics Medical Affairs . LOCATION: + The Medical/Scientific Director - Strategic… more
- AbbVie (Irvine, CA)
- …core R&D sub-functions, including Clinical Pharmacology & Pharmacometrics, Pharmacovigilance, Medical Affairs , Regulatory Affairs , and Clinical Development ... statistics, regulatory , etc.) as they relate to ongoing medical affairs projects. May assist as consultant/liaison with other corporations when working under… more
- AbbVie (Irvine, CA)
- …both US and International teams. Key Responsibilities: + Lead the development of the Global Medical Affairs medical content and training strategy for new hire ... onboarding, advanced training, and continuous training in Aesthetics. Work with Global Sci Comm, Medical Affairs , Medical Excellence and other cross-functional… more
- Medtronic (Irvine, CA)
- …**A Day in the Life** We are currently looking for a highly motivated Director of Biostatistics to join our Neurovascular Medical Science and Clinical Affairs ... programs, across multiple indications/therapeutic/disease areas within research and medical affairs . You will be accountable for strategic statistical input and… more
- AbbVie (Irvine, CA)
- …business objectives in a designated therapeutic area. As a member of the Global Eye Care Therapeutic Area Medical Leadership team and in partnership with Clinical ... will report directly to the VP of US & Global Pipeline Eye Care and is an integral part...execution of training, in conjunction with the Assistant Scientific Director and/or other members of the TA. Ensures the… more
- CSL Plasma (Anaheim, CA)
- …Staff Associates for completion of training and recommendation for certification by Regulatory Affairs . Functionally directs the Center Medical Staff. Provides ... as the primary center physician registered as the Laboratory Director with the Food and Drug Administration (FDA). **Job...CSL to reflect the world around us** As a global organization with employees in 35+ countries, CSL embraces… more
- AbbVie (Irvine, CA)
- …the regulatory requirements related to the clinical studies and global drug development and accountable for complying with those requirements. Serves as ... strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's customers, markets, business operations, and emerging issues.… more
- AbbVie (Irvine, CA)
- …the regulatory requirements related to the clinical studies and global drug development and accountable for complying with those requirements. May be ... strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's customers, markets, business operations and emerging issues.… more
- Fortive Corporation (Irvine, CA)
- …the position may encounter include: + R&D Directors, Quality, Operations, Marketing, Regulatory Affairs , Service and Support on project planning/execution + R&D ... Interactions** + This role will report to the Sr. Director of PMO + Potential internal interface activities that...full compliance with the QMS, FDA design controls, and global regulatory agency requirements. + Participate in… more
- Edwards Lifesciences (Irvine, CA)
- …and how our products transform patients' lives. As part of our Clinical Affairs team, you'll hone your scientific curiosity and passion for evaluating data to ... with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you will drive the evidence needed to optimize… more