Senior Scientist
vor 2 Monaten
**The Position**:
Boehringer Ingelheim develops cutting-edge viral therapeutics therapies with a focus on gene therapies, cancer vaccines and oncolytic viruses by combining its world class, in-house research and development with that of highly innovative external companies.
Join us to develop first-in-class immuno-oncology therapies for the benefit of our patients around the world.
This position is limited for 2 years.
***Tasks & responsibilities**:
- In your new role, you will lead and coordinate analytical activities (internal and external) associated to the development of a viral therapeutics, e.g. planning of studies, their execution and evaluation.
- As an expert, you will serve as the central point of contact for your project and ensure the timely processing of analytical topics by planning internal and external resources accordingly.
- Moreover, you will be responsible for the development and validation of methods for the release and stability testing of clinical trial preparations.
- In addition, you will independently prepare and present analytical chapters of regulatory documents towards health authorities.
- With your scientific expertise, you will support the development and qualification of analytical methods for release and stability testing of clinical material.
- As an analytical expert, you will represent analytical development in interdisciplinary and international project teams. You will also support process and formulation development with respect their analytical requirements.
- Based on your solid expertise, you will contribute to the overall analytical strategy, development of existing process and new analytical technologies.
**Requirements**:
- Master´s degree in Pharmacy, Biotechnology, Biology, Virology, Biochemistry or equivalent with long-term professional experience in a relevant field; PhD degree is preferable, with professional experience in the development or manufacturing of virus or protein therapeutics
- Sound leadership skills and experience in leading projects in multidisciplinary teams
- Very good expertise in analytical development and quality control of biopharmaceuticals in a GMP environment
- Sound knowledge of general GMP aspects and health authority guidelines/analytical requirements, preferably with a focus on ATMPs
- Team player with excellent communication, negotiation, presentation and organization skills (internal and external global interfaces)
- Agile, quick comprehension and high sense of quality and responsibility
- Strong matrix leadership skills, as well as independent, pragmatic and efficient working style
- Fluent English, written and spoken. Good German skills are preferable
**Ready to contact us?**:
Recruitment process:
Step 2: Virtual meeting in the period from end of September till mid of October
Step 3: On-site interviews end of October till beginning of November
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