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p>We are looking to strengthen our Workflow Team with a new team member!
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p>In this role, you will support workflow development by reviewing technical content, researching relevant information, and compiling structured documents.
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p>Your Tasks
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Review and summarize technical and regulatory information for analytical workflowsConduct research on industry trends, analytical techniques, and regulatory frameworksWrite and review technical articles for internal and external useSupport workflow development by compiling structured concepts and documentation
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p>Qualifikationen
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p>Your Profile
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University degree (Master's or PhD) in Natural Sciences (Chemistry, Pharmacy, Biology, Medicine)Hands-on experience with HPLC and LC-MS, as well as familiarity with other analytical techniques (e.g., GC-MS, NMR spectroscopy)Understanding of method validation, quality control, and regulatory frameworks for chemical analysis (e.g., FDA, DIN) and quality standards (ISO17025, ISO 17034 and ISO 9001).Knowledge of industry trends in chemical and pharmaceutical analysisExcellent writing and presentation skills in EnglishStrong team player with an independent, proactive, and organized working approachWork experience (â¥2 years) in a relevant field is an advantage