Analytical Project Leader Scientist

m/w/d, Basel-Stadt

This position on offer is located in Analytical Development Synthetic Molecules within Pharma Technical Development. Analytical Development is responsible for the development of resource and cost efficient analytical methods for all materials used during drug manufacturing using state of the art methodologies such as e.g. High-performance liquid chromatography (HPLC), Gas Chromatography (GC), Ion Chromatography (IC), Mass Spectrometry (MS), and others. The ultimate goal of our work is a robust control strategy to release pharmaceutical products for clinical trials, and finally for commercial supply

Responsibilities:

Cover all analytical aspects during the project development lifecycle
Work in close collaboration with peers, lab technicians and cross-functional partners from e.g. process development, material sciences, manufacturing, regulatory affairs, and quality assurance
Plan and document your experiments/results independently, and prepare for regulatory submissions such as IND (Investigational New Drug) and NDA (New Drug Application)
Be part of larger Technical Development Teams in which you regularly report out your progress
Collaborate with stakeholders from different disciplines, varying with the clinical phase of the project
Network closely with external partners such as CMOs and CROs (Contract Manufacturing/Research Organizations)

Requirements

Master or Ph.D. in chemistry, pharmacy, biotechnology or biochemistr
Minimum 3 years professional experience in the pharmaceutical industry
Experience in analytical development with Oligonucleotides, Peptides, biologically derived molecules and their advanced formulations is a plus
Knowledge in analytical methodologies such as e.g. PCR (Polymerase Chain Reaction) sequencing is a plus
• Strong quality mind-set and excellent attention to detail
Experience in applying GMP requirements where necessary, understanding how to exert them in different clinical phases

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