Analytical Project Leader Scientist

vor 5 Stunden

Basel, Schweiz TN Switzerland Vollzeit

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Analytical Project Leader Scientist, BaselClient:Location:Job Category:

Other

Job Reference:

49493506ab2f

Job Views:

7

Posted:

21.01.2025

Expiry Date:

07.03.2025

Job Description:

For our international medical partner, F. Hoffmann-La Roche Ltd. in Basel, we are looking for a qualified and motivated Technical Analytical Project Leader Scientist for a temporary contract of 12 months with the option to extend.

Behind every presentation of each product sold by Roche is the involvement of Pharma Global Technical Operations (PT). Starting with Phase I of the development process and continuing through to product maturity, PT makes medicines at sites around the world and includes more than 10,000 employees worldwide.

Global Technical Development (PTD) is an organization of over two thousand people globally that are integral for the mission of Roche to develop meaningful medicines for patients. Therefore, PTD actively collaborates and develops creative technical solutions to bridge early-stage, late-stage and commercial product needs. The mandate of the group is to reliably deliver the pipeline and supply quality products to patients. The group excels in its work through innovation, teamwork, dedication, and mutual respect and contributes every single day, continuously improving what it does.

Synthetic Molecules Technical Development (PTDC) brings a broad range of experience across drug substance (DS), drug product (DP), analytical sciences and Manufacturing Science & Technology (MS&T), and collaborates closely with key partners in the departments Research and Early Development (pRED / gRED), Small and Large Molecules (PTC, PTB), PTD and MS&T across our manufacturing network.

Tasks
  • 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)
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 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 able to respectfully collaborate with team members, customers and stakeholders, even in stressful situations
  • Fluent in English, German is a plus

Are you interested? Do not hesitate and submit your complete application documents online today.

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