Scientist Analytical Development 80-100 (f/m/d)

The actual location of this job is in Basel Stücki, Switzerland.

• Perform pharmaceutical development and analytical development studies for parenteral drug products of biologics (e.g. monoclonal antibodies, novel formats, ADCs) according to study protocols or other work instructions, including HPLC and CE purity methods, content by UV, identity, color, clarity and opalescence, pH, osmolality, extractable volume, CCI, visible particles, sub-visible particles and related drug product analytics.
• Follow applicable SOPs and current documentation practices.
• Ensure proper information flow related to assigned IRP tasks and contribute to departmental meetings and other departmental areas as needed.
• Maintain training status by completing required assigned trainings in a timely manner and attending on the job trainings (OJTs) and classroom trainings.
• Contribute to the upkeep of laboratory facilities and digital databases by engaging in periodic activities like cleaning and updates.
• Ensure proper maintenance of assigned equipment as IRP and other instruments in the laboratories.
• Adhere to relevant safety and health protection by following lab and safety instructions.
• Act as IRP (Instrument Responsible Person) including associated training tasks for assigned simple instrument(s), operate complex instruments with guidance.
• Manufacture, prepare and/or test non-GMP drug product samples for supportive stability studies and preclinical use (e.g. GLP tox studies), applying aseptic working techniques as applicable.