Scientist Qc-m

vor 2 Monaten


Martinsried, Deutschland Bavarian Nordic Vollzeit

Scientist (M/F/d) - Quality Control

**Join our transformative journey**:
At Bavarian Nordic, we aspire to save and improve lives by developing innovative vaccines that are designed to unlock the power of the immune system. We are a global leader in smallpox vaccines and our commercial product portfolio contains market-leading vaccines against rabies and tick-borne encephalitis as well as an Ebola vaccine. Our late-stage pipeline comprises a novel COVID-19 vaccine for boosting existing immunity and a vaccine against respiratory syncytial virus (RSV), for which no approved vaccines exist today.

We have embarked upon a transformative journey towards becoming one of the largest pure play vaccine companies by excelling in R&D innovation, manufacturing, and commercialization, and are looking for more talent to help drive the change. Come on board our journey and let’s change more lives, together.

**Become part of our growing QC department in Martinsried/Munich**:
The local QC department consists of about 45 colleagues who, together with a team situated in Denmark, form an important part of our quality organization. With your team you will release test clinical trial materials as well as our commercial products. You will also work closely with the team, that is dedicated to coordinating and testing of human clinical trial samples.

With a growing product portfolio that revolves around vaccines, you will also get the chance to contribute to the design and implementation of new methods and procedures along with our research department.

**Your responsibilities include**:

- Responsibility for the daily management of routine testing of GMP samples (FACS based virus titration, gene expression analysis, molecular biology, ELISA, AAS, GC) including assay monitoring and trouble shooting
- Maintenance and improvement of the GMP quality standard
- Participation in routine testing as required
- Method transfer, method validation and training of colleagues in analytical procedures
- Preparation and review of technical documents (e.g. SOPs, protocols, reports, CoAs)
- Preparation and review of quality related documents (Change Requests, Deviation Reports)
- Development of new QC assays
- Equipment qualifications

**About you**:

- Post-graduate (PhD) academic education in the bio/life sciences ideally with experience in virology/vaccine development
- Experience in development, optimization and validation of analytical methods compliant to international guidelines
- Preferably industry experience in daily business under GMP or GLP
- Good theoretical knowledge and practical experience in virological and cell-based analytical methods including standard cell culture techniques
- Advanced English and German communication skills

**We offer**:
A chance to work in an international company with unique technology and a dedicated work force. We offer a dynamic work environment and an opportunity to develop both your personal and academic competencies.
A chance to be a part of an international team with a strong work ethic but also a focus on a respectful and comfortable work environment.

**Caught your interest?**:


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