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Responsible for leading and managing pharmaceutical development projects of drug entities within Development Bioanalytics (DevBA) from various customers and in different pre-clinical development phases; Accountable
Responsible for supporting the execution of the global medical plan for the assigned product in collaboration with the rest of the global medical team, as well as supporting the necessary cross-functional workstreams, while adhering to the
Act as a subject matter expert (SME) for drug product (DP) manufacturing and validation activities; Lead and deliver MSAT projects focused on process optimization, robustness and cost improvements throughout the product lifecycle
Provide epidemiology and statistical analytical support for RWE studies; Contribute to the development of evidence generation plans and design of RWE studies for scientific and regulatory purposes; Advise study teams on research methodologies and