Flexsis is part of the Interiman Group, one of the leading providers of personnel services in Switzerland. Thanks to our solid expertise and the competencies within the Interiman Group, we offer customized solutions in personnel consulting. For our client Roche in Basel we are looking for a reliableAnalytical ScientistThe perfect candidate holds a Master's or Ph. D. in chemistry or pharmacy, coupled with a minimum of five years of experience within the pharmaceutical industry. A robust background in analytical development is paramount, with particular expertise in liquid chromatography and diverse detection methodologies.
Beyond technical proficiency,the person is an open-minded, goal-oriented individual who demonstrates the ability to thrive within a dynamic environment. The perfect candidate perceives challenges as opportunities for growth and consistently exhibits respectful collaboration with team members, customers, and stakeholders. Furthermore, an excellent command of the English language is a prerequisite. General Information: • Start date: asap• latest Start Date: 01. 12. 2025• Planned duration: 1 year• Extension: possible• Workplace: Basel• Workload: 100%• Home Office: Yes: max. 1 day per weekTasks & Responsibilities: Developing a phase-appropriate control strategy for pharmaceutical dosage forms, encompassing the active ingredient and its precursors.
Collaborating effectively with stakeholders across various departments, including drug substance and drug product process development and manufacturing, Technical Regulatory Affairs, Quality Assurance, and both internal and external analytical partners (such as service providers and commercial manufacturing/testing/packaging sites). Coordinating comprehensive analytical activities, which involves generating physical and chemical data for materials, developing/improving and validating analytical test methods or other analytical controls, generating packaging-specific stability data, and ensuring thorough documentation. Coaching technicians on project work and serving as a central point of contact for project-related information. Must Haves: A Master's or Ph. D.
in chemistry, pharmacy, or a related fieldA minimum of five years (ideally) of professional experience within the pharmaceutical industryProfound expertise in analytical development, encompassing formulation development support and the implementation of a control strategy for impurities in Investigational New Drug (IND) and New Drug Application (NDA) filingsA robust foundation in liquid chromatography (HPLC and UHPLC) with proficiency in various detection methods, including UV, Mass Spectrometry (MS), fluorescence, and charged aerosol detectionA comprehensive understanding of quality control principles is essential. Demonstrated experience in applying Good Manufacturing Practice (GMP) requirements and a clear understanding of their application across different clinical phases.
Are you interested? We are looking forward to receiving your application!
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