Analytical Project Leader Scientist (m/f/d)

With over 15 years of experience in the pharmaceutical and chemical industry as well as in biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated experts who want to develop professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – completely free of charge. Register with us and reap the benefits of interesting job offers that match your skills and experience.

Mein Arbeitgeber

• 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.
  

• 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)

• Master or Ph.D. in chemistry, pharmacy, biotechnology or biochemistry
• 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
• 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 are able to respectfully collaborate with team members, customers and stakeholders, even in stressful situation
• Fluent in English, German is a plus
  

• Join one of the world's leading pharmaceutical companies!
• Internal Career Opportunities
• International and Diverse Environment

Ihr Kontakt

Referenznummer
802088/1

Kontakt aufnehmen
Telefon:+41 44 225 50 00
E-Mail: positionen@hays.ch

Anstellungsart
Freiberuflich für ein Projekt