Analytical Associate in Analytical Development for Synthetic Molecules (m/w/d)

pFor one of our clients, a global pioneer in pharmaceuticals, we are currently looking for a dedicated bAnalytical Associate. /b /p pThis position is located within theb Analytical Development for Synthetic Molecules /b department, where cutting-edge techniques such as High-Performance Liquid Chromatography (HPLC), Gas/Ion Chromatography (GC/IC), and Mass Spectrometry (MS) are used to develop efficient and robust analytical methods. The goal is to ensure product release for clinical trials and subsequent commercial supply through a rigorous control strategy. /p h3General Information: /h3 ul libDuration: /b 1 year /li libExtension: /blikely /li libContract type: /b Temporary contract via Randstad (employment) /li libWork Location: /b Basel /li libHome Office: /b not possible /li libWorking Hours: /b Standard /li /ul h3Tasks Responsibilities: /h3 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 h3Must Haves: /h3 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) /li /ul h3Nice to Have: /h3 ul liKnowledge of GxP requirements and method validation /li /ul pTake a leading role in the development of innovative analytical techniques while contributing to the success of clinical and commercial therapies /p #J-18808-Ljbffr