Principal Scientist
35041 Marburg, Deutschland
Salary
Competitive
Start date
12 Aug 2020
Closing date
4 Sep 2020
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Discipline
Clinical Research
,
Clinical Research Scientist
,
R & D
,
Scientific
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)
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About CSL Behring
With operations in 35+ nations and ~ 22,000 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
Research
department we are looking for a
Principal Scientist (m/f/d)
(fulltime / permanent)Position Purpose
The position is located within the Research and Clinical Bioanalytics (RCB) department of CSL Behring Research. The facility provides regulatory compliant bioanalytical assays for the analysis of samples derived samples derived from early phase up to late stage development studies. We are highly dedicated to identify, implement and validate new, innovative technologies and state of the art methodology driven by our promise to care for our patients.As scientific expert in one of CSL’s therapeutic areas (TAs), preferably Cardiovascular & Metabolic (CV&M), the incumbent will contribute scientifically to existing projects as well as upcoming project opportunities.
As analytical expert especially in LC/MS-MS, Flow Cytometry, and cell based assays, her/his activities will furthermore involve supervising analytical work flows in a multitude of projects across all therapeutic areas. As such he/she assumes a leadership role in establishing cutting edge technologies in the (RCB) department under consideration of all relevant aspects of a regulated environment. The incumbent will ensure the ongoing identification and the development of state-of-the-art analytical technologies and their implementation into CSL’s research capabilities portfolio. This innovation process will be aligned with respective functionalities in CSL’s global research and development framework.
Main Responsibilities and Accountabilities
- Actively participate in the innovation process by identifying new opportunities, which could feed into the CSL development pipeline. Contribute to the development and progression of the global research project portfolio
- Take responsibility as RCB lead for selected projects e.g. as Bioassay Expert Team lead. Effective and transparent communication to laboratory team, colleagues and other key stake holders within CSL’s global R&D organization
- Actively collaborate with global, cross-continental project teams; and parties within and outside of own job function
- Contribute to CV&M TA by evaluating industry or academic opportunities identified by respective Research TA lead or Director of REI
- Keep updated with competitor landscape in relevant TA and contribute with novel and competitive analytical approaches
- Drive development of new capabilities to support all TAs
- Be strongly involved in and conduct of the day-to-day lab work
- Serve as function’s representative across early to late stage development activities
- Actively contribute to identify external partners in relevant techniques and support establishment of new collaborations
- Coach, train, review and delegate work to lower level professionals
Qualifications
- Post graduate qualification (typically PhD) in Molecular or Cell Biology, Biochemistry or associated fields
- Profound scientific knowledge to support CV&M TA
- Fundamental expertise in a broad spectrum of analytical technologies over a minimum of 7 years
- Ability to set up and optimize technologies on innovative analytical platforms
- Preferably deep technical and scientific background in cell based assays including Flow Cytometry and/or LC/MS-MS methodology and respective applications
- Understanding of working processes and requirements in a regulated environment (i.e. GxP)
- Track record of scientific and/or analytical achievements
- Managerial experience preferred
- Ability to work successfully and with limited oversight in a matrix organization structure
- Fluent in English and German (oral and written)
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