• Plan, execute and report results of scientific experiments for DS and/or DP applying state of the art analytical science and technologies (e.g., Release/stability/analytical method validation/ cleaning verification etc.) according to the agreed timelines. Ensure compliance to cGMP
• Accountable for documentation and submission of raw data in an appropriate system (e.g. LIMS)
• Responsible for good laboratory and documentation practices during execution of laboratory activities
• Support in evaluation and interpretation of results including investigations on SST failure, OOx/Deviation as required
• Review analytical documents (raw data review/approval, validation protocol, .....)
• Provide scientific guidance to laboratory associates
• Manage interactions and contribute to a high level of collaboration with internal and external stakeholders

• Master degree in analytical chemistry or equivalent and a minimum of 5 year's experience in the pharmaceutical industry
• Strong expertise in analytical techniques, e.g. HPLC, Particle size, Dissolution testing, cleaning validation/verification, X-Ray, IR, etc..
• GMP experience is a must
• On-Site assignment (no remote work possible)
• Experience with raw data review/approval
• Experience in handling Deviations/OOx as a plus
• Languages: Fluent in English, German as a plus

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