For our client, a leading company in the pharmaceutical sector, we are seeking an Analytical Scientist. In this role 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. This is an exciting opportunity to apply your expertise in a dynamic and challenging environment, contributing to the development of life-changing medicines. General Information: Start date: ASAPLatest Start Date: 01. 12. 2025Contract: temporary via RandstadPlanned duration: 1 yearExtension: possibleWorkplace: BaselWorkload: 80-100% (100% preferred)Home Office: up to 1 day per weekTeam: ca. 13 peopleDepartment:
Analytical Research & Development (MMDCA)Working hours: StandardTasks & 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 degree 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 essentialDemonstrated experience in applying Good Manufacturing Practice (GMP) requirements and a clear understanding of their application across different clinical phasesDigital 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 plusSuperior communication skills and a proven ability to collaborate successfullyOpen-minded, goal-oriented, and capable of thriving in a rapidly evolving environmentViews challenges as opportunities and consistently demonstrates respectful collaboration with team members, customers, and stakeholders, even under pressure
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