We are looking to strengthen our Workflow Team with a new team member!
In this role, you will support workflow development by reviewing technical content, researching relevant information, and compiling structured documents.
Your Tasks
Review and summarize technical and regulatory information for analytical workflows
Conduct research on industry trends, analytical techniques, and regulatory frameworks
Write and review technical articles for internal and external use
Support workflow development by compiling structured concepts and documentation
qualifications
Your Profile
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 analysis
Excellent writing and presentation skills in English
Strong team player with an independent, proactive, and organized working approach
Work experience (≥2 years) in a relevant field is an advantage