• Independently plan, organize, execute, and document scientific experiments (e.g., stability/ release testing, validations, etc.) according to the agreed timelines and appropriate quality standards.
• Execute experiments using HPLC, GC. Perform Cleaning validation and Cleaning verification experiments
• Accountable for documentation and submission of raw data in appropriate data system (e.g., GLIMS eLN ).
• Responsible for good documentation practices (GDP) and good laboratory practices (GLP) during execution of laboratory activities.
• Support in evaluation and interpretation of results including investigations on SST failures, OOX/Deviations/Change controls as needed.
• Responsible for assigned laboratory related area/activities (e.g., chemical/reagents/consumables /samples/column/ glassware management etc.).
• Train and coach associate scientists, technicians, temporary employees and employees under training / education
• Work according to appropriate SOPs, GMP, HSE, ISRM and the company’s Guidelines

• Bachelors/Masters in Life Science (e.g., analytical / organic chemistry /pharmacy / pharmaceutical development) or equivalent
• 3+ years of related experience in a GMP environment
• Experience with HPLC, Cleaning validation/verification, GC
• Understanding of general regulatory and quality expectations.
• Good scientific background, communication skills including presentation and scientific/technical writing.
• Languages: Fluent in English, German as a plus

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