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Biotechnologie: 3 Jobs in Sonnenbühl

Berufsfeld
  • Biotechnologie
Branche
  • Pharmaindustrie 3
Berufserfahrung
  • Mit Berufserfahrung 3
  • Mit Personalverantwortung 1
  • Ohne Berufserfahrung 1
Arbeitszeit
  • Vollzeit 3
Anstellungsart
  • Feste Anstellung 3
Biotechnologie

Senior Scientist Process Development (f/m/d) Drug Substance USP

Fr. 19.08.2022
Tübingen
CureVac AG is a global biopharmaceutical company researching and developing novel drugs based on the natural molecule Messenger RNA (mRNA). Our focus is on prophylactic vaccines, innovative cancer immunotherapies and protein-based therapies. Currently, all RNA people are striving to achieve our main goal: To bring multiple best-in-class mRNA drugs to market. To strengthen our team in Tübingen near Stuttgart, we are currently looking to recruit a Senior Scientist Process Development (f/m/d) Drug Substance USP Technical and disciplinary management of a team responsible for the development, optimization and upscaling of GMP-compliant manufacturing processes for RNA products Planning, execution, interpretation and documentation of experiments Overseeing and steering the development of biochemical characterizations of nucleic acids Subject-matter expert (SME) for process development topics at C(D)MOs as well as technology transfers to GMP production sites Preparation of development reports, risk analyses, laboratory instructions, training documents and SOPs Participation in interdisciplinary project teams PhD (or master's degree with several years of relevant working experience) in the field of biotechnology, pharmacy, biochemistry or chemistry, or a comparable qualification Extensive professional experience in the development of scalable and efficient biopharmaceutical processes; ideally in a pharmaceutical company Several years of relevant professional experience in the production of biopharmaceutical drug substances and process characterization Knowledge in bioreactor handling or tangential flow filtration Relevant knowledge in statistical experimental design and data analysis (DoE) Proactive, structured, efficient and independent way of working in a dynamic environment Strong communication skills and team-oriented work style Ability to independently devise research projects but also to work in an interdisciplinary team Fluency in English; German is a plus We offer you a challenging and varied opportunity with an innovative and dynamic company that is expanding. With much passion and sense of responsibility, we work together on the medical revolution. We pride ourselves on maintaining an honest and trusting relationship with each other which is characterized by openness to new ideas and continuous progress. Mutual respect, reliability and personal initiative are self-evident for us. Design your future with us – become part of the RNA people!
Zum Stellenangebot

Bioinformatician (f/m/d)

Do. 18.08.2022
Tübingen
CureVac AG is a global biopharmaceutical company researching and developing novel drugs based on the natural molecule Messenger RNA (mRNA). Our focus is on prophylactic vaccines, innovative cancer immunotherapies and protein-based therapies. Currently, all RNA people are striving to achieve our main goal: To bring multiple best-in-class mRNA drugs to market. As our next Bioinformatician (f/m/d) you will be a part of the cross-functional antigen validation team of the Target Discovery and Validation Center of CureVac Netherlands B.V. You will be working closely with your colleague bioinformaticians in Amsterdam and Tuebingen (Germany) on the development of mRNA based cancer vaccines. Contribute to the analysis of genomics, transcriptomics and proteomics data for the discovery of cancer antigens Support pre-clinical experiments aimed at validating specific antigens expressed in tumor cells In the context of clinical trials, provide extensive input with respect to tumor genomics analysis, design of vaccines, and statistical analysis of clinical and immunological data Design of novel vaccine strategies and collaboration with relevant (contract) research partners (universities, medical centers and biotech companies) Contribute to novel intellectual property to strengthen the patent position of CureVac, as well as attracting funding for collaborative research projects A BSc or MSc degree in Bioinformatics Experience in genomics & bioinformatics analyses of large sequencing datasets, preferable in the context of oncology Fluent in one or more scripting languages, such as Python, Perl, or Java (or similar languages) Able to quickly visualize research data in the form of clear figures or plots Experience with high-performance computing and Linux environments Experience with immunology would be a plus A highly motivated and driven attitude and an independent way of working Fluent in spoken and written English We offer you a challenging and varied opportunity with an innovative and dynamic company that is expanding. With much passion and sense of responsibility, we work together on the medical revolution. We pride ourselves on maintaining an honest and trusting relationship with each other which is characterized by openness to new ideas and continuous progress. Mutual respect, reliability and personal initiative are self-evident for us. Design your future with us – become part of the RNA people!
Zum Stellenangebot

Quality Manager Technical Development (f/m/d)

Fr. 05.08.2022
Tübingen
CureVac AG is a global biopharmaceutical company researching and developing novel drugs based on the natural molecule Messenger RNA (mRNA). Our focus is on prophylactic vaccines, innovative cancer immunotherapies and protein-based therapies. Currently, all RNA people are striving to achieve our main goal: To bring multiple best-in-class mRNA drugs to market. To strengthen our team in Tübingen near Stuttgart, we are currently looking to recruit a Quality Manager Technical Development (f/m/d) Finalize, revise and update SOPs in the area of development quality regarding Quality Target Product Profile (QTPP) and Drug Development Guideline (DDG) processes and their description Create and maintain SOPs of end-to-end process flow from TPP downstream to manufacturing authorization of commercial medicinal product via transfer (scale-up) and Process Performance Qualification (PPQ) runs, and define deliverables Formalize processes and get final approvals from all stakeholders Create, circulate, and approve SOPs, based on the feedback of the stakeholders Start establishing SOP training materials Define how to track any input to create and later change parameters in QTPP and other end-to-end processes Create QTPP history file electronically by participating in digitization projects of quality processes Alignment and integration of the QTPP process with DDG/TDG Match end-to-end process flow with required documents for documentation of the development history, and prepare signing off on the accomplishment of each stage gate review Support development programs regarding QTPP perspective to ensure adherence to the QTPP, and, if needed, initiate changes Foster and govern quality of TechDev in- and output, and its adherence to QTPP and DDG Master's or Ph.D. degree in in the field of biotechnology, pharmacy or chemistry, or a comparable qualification Several years of professional quality management experience in the (bio)pharmaceutical industry Experience in pharmaceutical-related regulated development and, preferably, CMC area Technical expertise in manufacturing and technical development is a plus Proven experience in working cross-functionally, leveraging their skills to influence and drive results within the matrix organization High self-steering capabilities and a structured way of working in a dynamic environment Exceptional team player and ability to develop strong network across the company project management skills Fluency in English and German We offer you a challenging and varied opportunity with an innovative and dynamic company that is expanding. With much passion and sense of responsibility, we work together on the medical revolution. We pride ourselves on maintaining an honest and trusting relationship with each other which is characterized by openness to new ideas and continuous progress. Mutual respect, reliability and personal initiative are self-evident for us. Design your future with us – become part of the RNA people!
Zum Stellenangebot


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