Analytical Project Leader Scientist

Vor 2 Tagen

Basel, Schweiz Randstad Switzerland Vollzeit

For our client, a leading company in the pharmaceutical sector, we are seeking a Analytical Project Leader Scientist.

This position 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 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.

General Information:

  • Planned duration: Project planned until 2028
  • Workplace: Basel
  • Home Office: max. 20%
  • Team: about 3-5 Team Members
  • Department: Analytical Research & Development (MMDCA)
  • Working hours: standard

Tasks & Responsibilities:

  • Cover all analytical aspects during the project development lifecycle
  • Work in close collaboration with peers, lab technicians, and cross-functional partners from 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)

Must Haves:

  • Master or Ph.D. in chemistry, pharmacy, biotechnology, or biochemistry
  • 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 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
  • Ideally experience of working in a paperless environment with strong IT skills to support digital transformation initiatives
  • Open-minded, goal-oriented, and able to work in a fast-developing environment
  • Takes challenges as opportunities and is able to respectfully collaborate with team members, customers, and stakeholders, even in stressful situations
  • Fluent in English, German is a plus
Seniority level
  • Mid-Senior level
Employment type
  • Contract
Job function
  • Project Management and Science
Industries
  • Staffing and Recruiting
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