Analytical Associate in Analytical Development for Synthetic Molecules

ppFlexsis is a company of the Interiman Group, one of the leading providers of personnel services in Switzerland. Thanks to our solid expertise as well as the competencies within the Interiman Group, we offer tailored solutions in personnel consulting. /p pFor our client bRoche /b in bBasel /b, we are looking for a reliable and motivated (m\/f\/d) /p h3Analytical Associate in Analytical Development for Synthetic Molecules /h3 ul liStart date: /li lilatest Start Date: /li liPlanned duration: 12 months /li liExtension: likely /li liWorkplace: Basel /li liWorkload: 100% /li liHome Office: No /li /ul ul liDevelopment 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). /li liPlanning and meticulous execution of experiments, including reaction monitoring and method development. /li liClose collaboration with process development and cross-functional partners to coordinate analytical activities and sample management. /li liClose cooperation with the QC (Quality Control) unit to ensure a smooth transfer of the developed analytical methods. /li liCreation of high-quality documentation, including analytical procedures and reports that serve as the foundation for method validations and regulatory filings. /li liApplication of an innovative mindset and digital tools for continuous improvement of analytical workflows in a dynamic environment. /li /ul ul liCompleted 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. /li liSolid practical experience with analytical instruments (e.g., HPLC, GC, KF, MS) as well as strong expertise in method development. /li liStrong scientific writing skills and the ability to summarize and present results of complex experiments precisely /li liHigh quality awareness and uncompromising attention to detail, including work within a non-GMP development environment /li liProactive, self-motivated work style and the ability to adapt quickly to new tools and processes in a dynamic team environment /li liFluent English language skills (both spoken and written) and German is beneficial. /li /ul h3Nice to Haves: /h3 ul liKnowledge of GxP requirements and method validation is an advantage. /li /ul /p #J-18808-Ljbffr