Job 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).
Minimum Qualifications 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 mindset 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.
Additional Information Join one of the world's leading pharmaceutical companies!
Internal career opportunities.
International and diverse environment.
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