3 - 4 Years Experience jobs in Austria (1), Belgium (4), Bulgaria (1), Croatia (1), Cyprus (1), Czech Republic (1), Denmark (1), France (8), Germany (8), Greece (2), Hungary (1), Ireland (5), Italy (4), Multiple Countries (8), Netherlands (2), Poland (10), Romania (1), Spain (5), Switzerland (7) and United Kingdom (7).
You will be responsible for providing medical safety expertise for the benefit/risk assessment of products in clinical development, with a specific focus on our key biologic (Nemolizumab). This involves signal detection, risk management
Responsible for developing and executing the Medical Affairs strategy in a selection of EU distributor markets where Insulet doesn’t have a direct presence in Europe. In conjunction with the Snr Medical Affairs Manager, the Medical Manager will be
In this role, you will contribute to the design, synthesis, and characterization of novel payloads, bioconjugation technologies, and linkers that enable innovative therapeutic modalities. You will work in a multidisciplinary environment
Lead drug product analytical investigations in close collaboration with the nitrosamines core experts and extended teams (both global and/or site experts). Serve as daily technical coach to nitrosamines analysts, and provide input and technical insights
Validate performance of new Agilent Automated Electrophoresis instrumentation and assays; Support quality of current products through corrective and preventative action (CAPA) investigations and continuous product improvement projects according to the
In this role, you will coordinate and track regulatory submissions, partnering with the Regulatory Lead to prepare high-quality global submissions and ensuring timely delivery to health authorities worldwide. You will provide operational support to
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.
You will oversee a team responsible for managing the end-to-end regulatory artwork process for pharmaceutical and non-pharmaceutical products across Europe. In addition to your leadership responsibilities, you’ll remain actively involved in daily