As Analytical Scientist, you will be joining a highly motivated and experienced team of analytical scientists. You will be responsible for leading analytical development activities for synthetic molecule projects, from early development to commercialization. The 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. General Information: Start date: asap, but latest date: 01. 12. 2025Planned duration: 1 year, extension possibleWorkplace: BaselWorkload: 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 precursorsCollaborating 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 documentationCoaching technicians on project work and serving as a central point of contact for project-related informationMust Haves:
A Master's or Ph. D.
in chemistry, pharmacy, or a related fieldMinimum 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 essentialDemonstrated experience in applying Good Manufacturing Practice (GMP) requirements and a clear understanding of their application across different clinical phases.
Digital acumen to support digital transformation initiatives; familiarity with statistical analysis of analytical data is also advantageousExcellent command of the English language. Proficiency in German is considered a plusViews challenges as opportunities and consistently demonstrates respectful collaboration with team members, customers, and stakeholders, even under pressureDeadline for submission: 06/08
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