Technician Early Translational Sciences (ETS) in München bei Novartis

2023 will potentially see Sandoz become a standalone organization! Already a global market leader in Generics and Biosimilar medicine, this is an exciting, once-in-a-career opportunity to set our own path forward as an independent, purpose-driven organization, and as the founders of a new Sandoz, this is a time of immense opportunity for us all, both professionally and personally!

Together we will shape the future of Sandoz… are you ready to make a difference?

8 biosimilars across immunology, oncology and endocrinology are already on the market, Sandoz Biopharmaceuticals has a leading biosimilars pipeline with additional molecules in various stages of development. As Preclinical Development Manager, you contribute to the future success of our biosimilar development. You are responsible for providing nonclinical expertise to assigned global cross-functional biosimilar program teams, leading the timely planning and execution of innovative and tailored nonclinical development programs

Your key responsibilities:
Your responsibilities include, but not limited to:

• Plan, organize, perform and document scientific experiments/activities, e.g. the development and qualification of in vitro cell-based and immunoassays for functional protein characterization, under supervision/in collaboration with experienced team members.
• Manage operational aspects in lab:
• Schedule and perform maintenance, qualification, calibration and cleaning of analytical instruments/equipment.
• Actively maintain laboratory inventory (e.g. chemicals, standards, consumables) within own area of responsibility.
• Work according to appropriate standards as defined in Quality Manual, SOPs, ethical, health, safety, environment (HSE), and information security (ISEC) guidelines.
• Provide documentation of raw data, evaluate results for method development and/or qualifications, routinely applied methods or procedures. Follow organizational procedure.
• Support interpretation and reporting of results and troubleshooting, if needed.
• Support optimization of existing methods/processes.
• Write documents, e.g. basic laboratory procedures / SOP’s or study plans and reports based on templates under supervision.
• Contribute to report writing (e.g. by preparation of tables and figures).
• Address and solve problems within own assigned area of responsibility. Recognize and communicate issues (e.g. deviations and unexpected results from experiments).
• Contribute to development of new methods/processes and reproduce published methods/processes or optimize existing methods under supervision.
• Collaborate within own and with other groups.
• Actively participate in knowledge exchange.

Commitment to Diversity & Inclusion:

Minimum requirements