Analytical Associate in Analytical Development for Synthetic Molecules

Flexsis is part of the Interiman Group, one of the leading providers of personnel services in Switzerland. Thanks to our solid expertise and the competences within the Interiman Group, we offer tailor-made solutions in personnel consulting.For our client Roche in Basel, we are looking for a motivated and reliable (m/f/d)Analytical Associate in Analytical Development for Synthetic MoleculesThe Perfect Candidate: holds a solid vocational qualification or a bachelor’s degree in Analytical Chemistry, Biochemistry, Biotechnology, or a related field, with 1–3 years of hands-on experience in analytical method development within the pharmaceutical industry. They are proficient in analytical techniques such as HPLC, GC, and KF, apply GxP principles confidently, and possess strong scientific writing and documentation skills. With an innovative and quality-driven mindset, they demonstrate adaptability, digital fluency, reliability, and a proactive, collaborative approach in a dynamic environment.General Information:• Start Date: 01.12.2025• Latest Possible Start Date: 01.01.2026• Planned Duration of Employment: 12 months• Extension (for temporary contracts): extension need to be discussed• Workplace: Basel• Workload: 100%• Home Office: NoTasks & Responsibilities:Development, improvement and validation of analytical methods for the quality assessment of starting materials, intermediates, reaction monitoring, active substances and galenical forms.Thorough and efficient planning, execution and documentation of experiments in collaboration with the relevant team members, analytical project lead and your supervisor, following current GxP guidelines as well as the relevant SOP’s.Work on end to end processes in close collaboration with other associates, scientists, and partners from other departments to ensure efficient analytics and continuous improvement.Coordination of analytical activities including sample management for the development of synthetic products.Authoring of documents, e.g. analytical procedures, and validation reports.Routinely apply GxP requirements where necessary, and understand how to exert them in different clinical phases.Must Haves:You hold a solid vocational qualification with at least 1-3 years’ experience in the pharmaceutical industry with a strong focus on analytical methods development (i.e. chromatography) or a bachelor's degree (Analytical Chemistry, Biochemistry, Biotechnology or related field). The role does not require any further academic qualifications. Hands-on experience in analytical instrumentation and techniques (e.g. HPLC, GC, KF)Routinely apply GxP requirements where necessary, and understand how to exert them in different clinical phases. Excellent command of English. Good command of German would be a plus.A strong interest / background in analytical methods development.A good scientific writing style and good documentation practice for utilization of corresponding data in regulatory filings.Are you interested and would you like to seize this opportunity? Then we should definitely get to know each other! Simply click on "Apply now" and we look forward to receiving your complete application documents