Principal Scientist_process development
vor 15 Tg.

At Lonza, we invest in great people. We encourage our employees to challenge themselves and we offer an environment that fosters creativity and success.

Headquartered in Basel, Switzerland, we operate production, R&D, and business sites around the world, including Europe, North America, and Asia.

Our vision :

We strive to be the leading supplier using science and technology to improve the quality of life.

Our mission :

We work with passion, using advanced technologies, to transform life science into new possibilities for our customers.

Do you want to help us as we shape the future of this great organization?

Job Description Summary

Provide Scientific and technical expertise in the DPS Process development group for projects involving biologics and small molecule and peptide parenteral products.

Support manufacture of pre-clinical as well as clinical drug product supplies.

Key Accountabilities and Duties

  • Support the build-up and establishment of drug product process development services for parenteral products incl. infrastructure and equipment.
  • Identify, evaluate and procure drug product process development laboratory capabilities (10%)

  • Design and implement scale-down models for the development and characterization of drug product manufacturing process unit operations, and create scale-
  • up tools. Implement phase appropriate generic study stages for process development.(30%)

  • Participate in multi-disciplinary project teams and lead sub-teams as per need. Plan and perform process development and characterization studies for liquid and lyophilized parenteral drug products of biologics (e.
  • g. monoclonal antibodies, novel formats, ADCs, peptides), peptides and small molecules (20%)

  • Support the scale-up and technology transfer for drug product manufacturing at internal and / or external manufacturing sites.
  • Support manufacture of clinical drug supplies at GMP sites (10%)

  • Responsible for authoring technical documents and support preparation of regulatory documentation. (10%)
  • Ensure safety and health protection following lab and safety instructions
  • Enable innovation and technical strategy projects, generate IP and contribute to scientific publications and presentations.
  • Also represent and promote Lonza at industry events as required (10%)

  • Collaborate across drug product services (DPS) and the whole of Lonza Pharma Biotech (LPB), e.g., with analytical, formulation, QC and manufacturing functions. (10%)
  • Perform other duties as assigned.
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