Development and optimization of robust analytical methods (HPLC, GC, LC-MS, GC-MS, KF) für die Qualitätsbewertung von Ausgangsmaterialien, Zwischenprodukten und aktiven pharmazeutischen Wirkstoffen (APIs)
Planning and meticulous execution of experiments, including reaction monitoring and method development
Close collaboration with process development and cross-functional partners to coordinate analytical activities and sample management
Close cooperation with the QC (Quality Control) unit to ensure smooth transfer of developed analytical methods
Creation of high-quality documentation, including analytical procedures and reports
Application of an innovative mindset and digital tools for continuous improvement of analytical workflows

Completed vocational training in natural sciences (Laboratory Technician) or Bachelor's degree in Chemistry, Biochemistry, or related field with at least 2-3 years professional experience in pharmaceutical industry
Solid practical experience with analytical instruments (HPLC, GC, KF, MS) and strong expertise in method development
Strong scientific writing skills and ability to summarize and present results of complex experiments precisely
High quality awareness and uncompromising attention to detail in non-GMP development environment
Proactive, self-motivated work style and ability to adapt quickly to new tools and processes in dynamic team environment
Fluent English language skills (spoken and written), German beneficial
Knowledge of GxP requirements and method validation is an advantage

Analytical Associate in Analytical Development for Synthetic Molecules

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