Beschreibung
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 (â¥2 years) in a relevant field is an advantage