Analytical Associate in Analytical Development for Synthetic Molecules

ph3Description of the company /h3 /brpFlexsis 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 /brpFor our client bRoche /b in bBasel /b, we are looking for a reliable and motivated (m/f/d) /p /brh3Analytical Associate in Analytical Development for Synthetic Molecules /h3 /brul /brliStart date: /li /brlilatest Start Date: /li /brliPlanned duration: 12 months /li /brliExtension: likely /li /brliWorkplace: Basel /li /brliWorkload: 100% /li /brliHome Office: No /li /br /ul /brh3Role Responsibilities /h3 /brul /brliDevelopment 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 /brliPlanning and meticulous execution of experiments, including reaction monitoring and method development. /li /brliClose collaboration with process development and cross-functional partners to coordinate analytical activities and sample management. /li /brliClose cooperation with the QC (Quality Control) unit to ensure a smooth transfer of the developed analytical methods. /li /brliCreation of high-quality documentation, including analytical procedures and reports that serve as the foundation for method validations and regulatory filings. /li /brliApplication of an innovative mindset and digital tools for continuous improvement of analytical workflows in a dynamic environment. /li /br /ul /brh3Candidate Profile /h3 /brul /brliCompleted 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 /brliSolid practical experience with analytical instruments (e.g., HPLC, GC, KF, MS) as well as strong expertise in method development. /li /brliStrong scientific writing skills and the ability to summarize and present results of complex experiments precisely /li /brliHigh quality awareness and uncompromising attention to detail, including work within a non-GMP development environment /li /brliProactive, self-motivated work style and the ability to adapt quickly to new tools and processes in a dynamic team environment /li /brliFluent English language skills (both spoken and written) and German is beneficial. /li /br /ul /brh3Nice to Haves: /h3 /brul /brliKnowledge of GxP requirements and method validation is an advantage. /li /br /ul /p #J-18808-Ljbffr