Descripción
Tasks & Responsibilities: • Development and optimization of robust analytical methods (e.g., HPLC, GC, LC-MS, GC-MS, KF) for the quality assessment of starting materials, intermediates, and active pharmaceutical ingredients (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 a smooth transfer of the developed analytical methods. • Creation of high-quality documentation, including analytical procedures and reports that serve as the foundation for method validations and regulatory filings. • Application of an innovative mindset and digital tools for continuous improvement of analytical workflows in a dynamic environment. Must Haves: • Completed vocational training in natural sciences (Laboratory Technician) or a Bachelor's degree in Chemistry, Biochemistry, or a related field with at least 2-3 years of professional experience in the pharmaceutical industry. (*****) • Solid practical experience with analytical instruments (e.g., HPLC, GC, KF, MS) as well as strong expertise in method development. (*****) • Strong scientific writing skills and the ability to summarize and present results of complex experiments precisely. (*****) • High quality awareness and uncompromising attention to detail, including work within a non-GMP development environment. (*****) • Proactive, self-motivated work style and the ability to adapt quickly to new tools and processes in a dynamic team environment. • Fluent English language skills (both spoken and written) and German is beneficial.