Senior Scientist - Virus Validation

CSL Behring GmbH (DE) (Marburg HE, Deutschland) Vor 7 Tagen veröffentlicht

With operations in 35+ nations and ~ 27,000 employees worldwide, CSL is driven to develop and deliver a broad range of lifesaving therapies to treat disorders such as hemophilia and primary immune deficiencies, and vaccines to prevent influenza. Our therapies are also used in cardiac surgery, organ transplantation and burn treatment.

CSL is the parent company of CSL Behring and Seqirus. CSL Behring is a global leader in the protein biotherapeutics industry, focused on bringing to market biotherapies used to treat serious and often rare conditions. CSL Behring operates CSL Plasma , one of the world's largest collectors of human plasma, which is used to create CSL’s therapies. Seqirus is the second largest influenza vaccine company in the world and is a transcontinental partner in pandemic preparedness and a major contributor to the prevention and control of influenza globally.

We invite you to take a look at the many career possibilities available around the globe and consider building your promising future at CSL by becoming a member of our team!

For our Global Pathogen Safety department we are looking for a

Senior Scientist Virus Validation (m/f/x) - R-125711

(Fulltime / regular)

Main Responsibilities and Accountabilities:

  • Staff Management: Planning of resources and leading of team meetings

  • Execution of performance and development reviews, derivation of next steps if necessary

  • Monitoring the training status of the direct reports and securing the safety requirements and working hours regulations within the area of responsibility

  • Evaluation of direct reports regarding hiring/contract renewal and salary grouping (tariff)

  • Interviewing for open positions

  • Development of experimental study designs

  • Planning and execution of experiments including data analysis and communication of the results usually to the project team in the form of a report or presentation

  • Development of state-of-the art experimental methods and processes

  • Promotes research and communication initiatives across departments

  • Evaluation of experimental data and derivation of next steps

  • Operation of complex devices, program scripting, processing and preparation of raw data

  • Presentation of experimental results in internal and external meetings

  • Contributions at congresses and preparation of publications

  • Contributions to research projects and taking responsibility for sub steps

  • Identification of relevant technologies or platforms for research and product development activities

  • Collaboration in the budget planning for R&D projects

  • Coordination of project and study planning with other areas (e.g. manufacturing, quality assurance) or other locations

  • Discussion of results with other areas (e.g. manufacturing, quality assurance) or other locations

  • Collaboration or coordination of task forces

  • Contact and obtain information from external vendors and collaboration partners

  • Ensure that colleagues are familiar with processes and equipment

  • Generation and maintenance of records in internal documentation systems

  • Providing written reports for official documents (e.g. approval applications for active substances)

  • Write and revise technical documents, including work instructions, test or process logs, and reports (including submission relevance, if any).

Experience in the following areas is an advantage:

  • Practical work with cells and viruses under biosafety level 2 conditions or higher

  • Studies to determine the pathogen (e.g. virus, prion) clearance capacity of biopharmaceutical products

  • Good Laboratory Practice

Qualifications & Experience:

  • A University Degree in a relevant field of Science (e.g. Master of Science in biology)

  • Project experience and knowledge of relevant analytical methods

  • English Level 2

  • 1-3 years of relevant experience

Marburg, 19.11.2020

CSL Behring GmbH - Human Resources


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Senior Scientist - Virus Validation

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