Jorg Blumel, PhD

Global Biopharma Executive || Translational Science Leader || Senior Vice President, Global Head Development Sciences

San Francisco Bay Area

About

Accomplished executive leader and seasoned drug development professional with more than two decades of biopharmaceutical industry experience in global organizational leadership roles in US & Europe. Proven expertise in leading and scaling global, multi-disciplinary organizations successfully delivering innovative scientific approaches and end-to-end nonclinical and translational drug development strategies for biopharmaceuticals, synthetic molecules, complex therapeutic modalities, and medical devices. Recognized for a visionary, strategic enterprise mindset and documented success in pioneering transformative organizational strategies and complex change management initiatives. Inspiring people leader dedicated to cultivating high performing teams and trusted mentor promoting personal growth and career development. Successful track record of advancing innovative therapeutic modalities from discovery through preclinical development and First-in-Human trials, culminating in successful global market authorizations.

Experience

  • Genentech (South San Francisco, CA · On-site)
    • Senior Vice President, Global Head Development Sciences
      Nov 2022 - Present · 3 yrs 8 mos

      Accountability for strategic, scientific and organizational leadership of four major departments with global responsibilities for Nonclinical and Translational Safety Assessment, BioAnalytical Sciences, Clinical Pharmacology, and Preclinical & Translational PKPD.

    • Vice President, Head Safety Assessment
      May 2019 - Oct 2022 · 3 yrs 6 mos

      Head of Nonclinical Safety Assessment spanning Nonclinical Operations, Toxicological Pathology, Toxicology and Occupational Toxicology Functions.

    • Head Development (Regulatory) Toxicology and Product Quality/ Occupational Toxicology
      Aug 2016 - Apr 2019 · 2 yrs 9 mos

      Head of the Regulatory Toxicology and Product Quality/ Occupational Toxicology groups.

  • Director Biologics Safety Assessment at MedImmune
    Oct 2011 - Aug 2014 · 2 yrs 11 mos

    Oversight of bio-superior biopharmaceuticals portfolio, cross-functional translational sciences team lead and global toxicology project lead.

  • Merz Pharmaceuticals (On-site)
    • Head Nonclinical Safety / Drug Metabolism
      Jan 2006 - Sep 2011 · 5 yrs 9 mos

      Head of Nonclinical Safety, Nonclinical DMPK, the GLP-certified Biological Analytics, and Laboratory Animal Sciences.

    • Head Toxicology
      Feb 2001 - Dec 2005 · 4 yrs 11 mos

      Group leader Toxicology and Safety Pharmacology.

  • Research Scientist at Xerion Pharmaceuticals
    Apr 2000 - Jan 2001 · 10 mos