About this role
Your Responsibilities* Development and optimization of robust analytical methods ( 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* Cooperation with the QC unit to ensure smooth transfer of developed analytical methods* Preparation of high-quality documentation, including analytical procedures and reports supporting method validation and regulatory submissions* Use of innovative approaches and digital tools to continuously improve analytical workflowsMust-Have Qualifications* Completed vocational training as a Laboratory Technician (Chemielaborant) or Bachelor's degree in Chemistry, Biochemistry, or a related scientific discipline* Minimum 2-3 years of professional experience within the pharmaceutical industry* Strong hands-on experience with analytical instrumentation such as HPLC, GC, KF, and MS* Proven experience in analytical method development* Excellent scientific writing and documentation skills* High quality awareness and exceptional attention to detail* Proactive and self-driven working style* Fluent English (written and spoken)* German is considered an advantageNice-to-Have Qualifications* Knowledge of GxP requirements* Experience with analytical method validation* Previous experience in analytical development within pharmaceutical manufacturing or process development environmentsThe Ideal CandidateYou are a hands-on analytical scientist or laboratory technician with a passion for method development and problem-solving. You enjoy working in a dynamic development environment, collaborate effectively across functions, and bring a strong focus on quality, documentation, and scientific excellence.j4id10444953jm j4it1042jm j4iy26jm