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Accountable for Protein Reagent supply and Profiling to early drug discovery projects. Provide scientific direction and supervision of a project and scientific capability portfolio, not only through direct involvement but may also via mentoring/coaching
In this role, you will be responsible for managing a team of Quality Assurance and Quality Control Specialists, oversee customer and regulatory audits, be QC named responsible person to maintain our MHRA license, overseeing batch release of GMP batches,
Develop and drive the nonclinical PKPD strategy for projects. Ensure translation from in vitro data and in vivo nonclinical studies to prediction of efficacy and safety in patients. Build PKPD models of sufficient complexity to allow hypothesis testing