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Biotechnology and Genetics jobs in Belgium (1), Croatia (1), France (3), Germany (6), Greece (6), Ireland (1), Netherlands (1), Poland (1), Switzerland (8) and United Kingdom (9).
Your main tasks will include the development and adaptation of single use accessories for the CliniMACS Prodigy and CliniMACS Plus systems. As the group leader, you will take on both technical and disciplinary leadership responsibilities for a dedicated
Design and execute formulation strategies for biosimilar products including monoclonal antibodies, fusion proteins, and other biologics. Plan and oversee pre-formulation studies, stability testing, and compatibility assessments. Lead and mentor a team of
In this role, you’ll provide global scientific and technical leadership, contribute to innovation strategies, and act as a thought leader - both within Lonza and the wider biopharmaceutical industry. Guide development of mammalian USP/DSP processes for
Responsible for all tasks and resources including cross functional co-ordination required to complete relevant QC microbiology activities within regulated environment in the required timeframe. Management of QC Microbiology team to carry out tasks.
Lead key projects in mammalian cell line development, while spending the majority of your time (~80%) performing hands-on lab work; Mentor and support junior scientists within the team, fostering skill development and knowledge sharing; Contribute to the
Lead the full lifecycle of complex programs from contract signature to delivery. Act as the single point of contact for customers and advocate for their needs on-site. Ensure delivery on time, within budget, and to the highest quality standards.
In this role, you will be responsible for applying biology knowledge in an engineering environment to support product development of novel systems used in biopharmaceutical development. This involves working in a multidisciplinary team to achieve the
Mit dem Themenfeld der neuartigen Therapien und den regulatorischen Anforderungen an die Herstellung und Prüfung entsprechender Arzneimittel sind Sie vertraut; Zudem haben Sie bereits Erfahrung mit der Akquise und/oder Umsetzung von GMP-Beratungs- und
You will be responsible for the implementation, development and validation of high-quality qPCR, dPCR and NGS assays for use in clinical trials utilizing state of the art RNA and DNA technologies. Conduct laboratory procedures to support the development
Independently plan, organize, perform and document experiments for the development and qualification of in vitro cell-based bioassays and immunoassays for functional characterization of biosimilars in alignment with the nonclinical in vitro strategy of
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