Jobdescription
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
Qualifikationen
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