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Serve as an expert in drug development capable of advising on strategic decisions and directing resources. Build relationships with external parties relevant to ExploR&D development. Drive global solutions with the broader ExploR&D team and business
Root cause analysis (RCA) and CAPA implementation for project topics, and general lab topic. Investigation and management of deviations, as Lead Investigator. Quality oversight and audit readiness in GMP-regulated labs (participation in audits for
Responsible for shaping and executing the R&D strategy within the oncology therapeutic area as well as leading strategic partnerships in the field. This role drives innovation, identifies high-impact opportunities, and steers cross-functional efforts to
You'll be the primary regulatory CMC voice on cross-functional matrix teams, covering everything from early clinical trial applications through to new marketing authorizations, post-approval changes, and full lifecycle management. That means you won't
Lead and execute MSAT projects such as manufacturing process and cost improvement as part of LCM; Participate in internal activities related to (external) manufacturing such as process changes, major/critical deviations, risk assessments and CAPAs;