Senior Scientist Process Development Drug Product 12 months fix-term contract

Assist establishment of Drug Product process development infrastructure and services for parenteral drug products for clinical and commercial use Install, qualify, and maintain equipment for process development, non-GMP manufacturing and related analytics in close alignment with current best practices and regulations 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 Supervision of the junior scientists or interns when required Document data following applicable lab procedures and current documentation practices Good understanding on Annex1 and the implication on GMP Drug product manufacturing process (e.g. Filtration, Mixing and Compounding, Hold-time, Ambient light, VHP uptake) Support manufacture of non-clinical and clinical drug supplies at GMP sites

At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of. Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.

• Science or engineering degree (BSC or MSc) in a relevant discipline, e.g. Pharmaceutical Sciences, Chemical or Biochemical Engineering

• Minimum 3 years of experience in pharmaceutical or chemical industry, preferably in process development

• Working experience in relevant pharmaceutical development and manufacturing technologies. Experience with parenteral dosage forms, protein formulation and analytics and aseptic working techniques is a plus

• Very good knowledge of reporting, interpretation and documentation of scientific results

• Experience with parenteral dosage forms and/or lyophilization techniques is a plus

• Ability to work independently in a team environment, with attention to detail and proactive attitude. Good knowledge of written and spoken English. Any other languages are a plus