- 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
- Edwards Lifesciences (Irvine, CA)
- …to regional commercial and marketing groups as well as functional stakeholders including regulatory , medical affairs , clinical affairs , legal, public ... continue to enable us to transform patient lives around the world. The Senior Director will lead the US regional compliance team and oversee the US compliance… more
- AbbVie (Irvine, CA)
- …Stakeholders + Clinical development experts + Statistical programmers + Data science experts + Global Medical Affairs experts + Regulatory experts *This role ... and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Associate Director / Director , Statistics provides scientific and statitical leadership for… more
- AbbVie (Irvine, CA)
- …May coordinate and develop information for reports submitted to the FDA and Global Regulatory Authorities. + Leads cross functional sub-teams responsible for ... as an assistant Principal Investigator or Principal Investigator. + Direct experience with regulatory bodies (FDA and Global regulatory agencies) is highly… 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
- Charles River Laboratories (Northridge, CA)
- …you will make a difference every day. **Job Summary** **SUMMARY** The Director , Manufacturing Operations is responsible for the Manufacturing Operations of multiple ... Work flows and processes should be mapped and undated to align with global practices as applicable. Assist direct reports to maximize productivity and efficiency… more
- AbbVie (Irvine, CA)
- …strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's customers, markets, business operations, and emerging issues. ... of investigators, study site personnel, and AbbVie study staff. + Lead global clinical study teams monitoring overall study integrity and review, interpretation, and… 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
- AbbVie (Irvine, CA)
- …8-12 years' experience in the pharmaceutical industry in Clinical Development, Regulatory Affairs , Commercial or Pharmaceutical Development areas including ... coordination and management (organization, planning, execution, monitoring, and control) of global R&D projects to which he/she is assigned. He/she is accountable… 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
- Fortive Corporation (Irvine, CA)
- …+ Work together with engineering, project management, manufacturing, quality, planning, marketing, regulatory affairs , and suppliers to identify and drive total ... best practice. This role will work closely with the Director of Strategic Sourcing and category leaders in deployment...or medical field. + 5+ years of experience in global and complex manufacturing procurement or supply chain management.… more
- AbbVie (Irvine, CA)
- …serves as a key contact and advocate between various internal stakeholders (eg, Regulatory Affairs , Medical Safety, Medical Writing, PMQA, etc.) and drives ... on management of the supporting post-market processes, and reports to the Director , Medical Device & Combination Products Shared Services (or equivalent). The… more