Pre-clinical Research and Development jobs in Europe involving the drug discovery and design process. R&D jobs as a biochemist, geneticist, immunologist, medical chemist, microbiologist, molecular biologist, organic chemist, pharmacologist, scientist, toxicologist, including those in research institutes and universities. Find more pre-clinical research jobs on EuroScienceJobs.
Pre-clinical Research and Development jobs in Belgium (4), Cyprus (2), Denmark (1), France (2), Germany (11), Ireland (14), Italy (4), Lithuania (4), Malta (1), Multiple Countries (5), Netherlands (7), Poland (5), Portugal (1), Spain (4), Sweden (1), Switzerland (13) and United Kingdom (15).
Drive biomarker testing strategies across multiple clinical trial programs as well as diagnostic and companion diagnostic (CDx) initiatives; Act as a scientific expert in selecting fit-for-purpose analytical technologies such as LC-MS...
Lead and develop a multidisciplinary team of process engineers, specialists, and manufacturing professionals, fostering a culture of safety, quality, accountability, and continuous improvement. Take ownership of operational performance within the DSP
Lead and execute MSAT projects such as manufacturing process and cost improvement as part of LCM; Participate in internal activities related to (external) manufacturing such as process changes, major/critical deviations, risk assessments and CAPAs;
Root cause analysis (RCA) and CAPA implementation for project topics, and general lab topic. Investigation and management of deviations, as Lead Investigator. Quality oversight and audit readiness in GMP-regulated labs (participation in audits for
You will identify compliance gaps, guide investigations, and lead improvements that support reliable laboratory processes. You will also share your expertise and help teams prepare for regulatory inspections. Lead improvement projects with QC, Quality
Responsible for supporting the development, coordination, and execution of cutting-edge, effective, and efficient real world evidence strategy for drug and enablement projects at global level or for key critical markets. He/she works in close partnership
Responsible for leading non‑clinical and early clinical pharmacology strategy across drug development programs. Provides expertise in PK/PD, modeling & simulation, and Model‑Informed Drug Development (MIDD) to support dose selection, study design, and
Develop bioanalytical (especially LC/MS/MS) methods for the discovery and development of NCEs (New Chemical Entities) or NBEs (New Biological Entities). Operate and maintain LC-MS/MS instrumentation, ensuring proper calibration, troubleshooting, and
Lead the project management efforts for Research and Development projects through design, development and taking to market of medical devices. Manage the key activities of the project and drive project tasks to ensure timely completion of project
Provide strategic and operational leadership for the Bioanalysis and Immunoanalysis/Immunogenicity groups, ensuring alignment with Ipsen’s R&D and business objectives; Oversee the management, development, and continuous improvement of the Dreux
Lead the design and computational optimisation of RNA therapeutics, particularly siRNA, integrating RNA biology with oligonucleotide chemistry to enable gene knockdown and RNA regulatory approaches, including up-regulation strategies; Define and
The ideal candidate must possess a solid foundation/expertise in Immunology with a proven track record of building cross-disciplinary teams and working cross-functionally to deliver large molecule portfolio assets to the clinic. Serve as a
This role will be pivotal in ensuring all products manufactured meet the standards required for marketed drug products. They will be accountable for defining contamination control strategy and its sterility assurance practices and sever as a subject
Provision of scientific and technical leadership to multidisciplinary teams to achieve corporate goals in challenging research projects within early-stage biologics drug development. Developing, executing and optimizing protein production processes
Ensure highest quality standards are maintained in areas of responsibility and that industry best practice is adopted in accordance with current GLP, GMP and regulatory body directives; Ensure all laboratory analysis is carried out in a safe
In this role, you will perform analytical method development, optimization, validation activities and stability testing supporting pharmaceutical development of drug products. You will combine strong technical expertise with scientific problem-solving and
Accountable for leading an injectable analytical group: developing, validating methods, characterizing structures of peptides and complex injectables with state of the art techniques. Preparing technical reports to demonstrate structural and impurity
Manage day-to-day laboratory activities for assigned formulation projects, providing guidance and support to scientists to ensure high-quality scientific delivery. Ensure laboratory practices comply with SOPs, quality standards, IOPs, and Health & Safety
In this role, you will support Servier’s research pipeline by contributing to strategic data management projects, ensuring that our preclinical data is a trustable asset for life-changing therapeutic innovation. Ensure data integrity within your
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