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 (9), Croatia (2), Cyprus (1), Denmark (3), France (15), Germany (14), Greece (3), Ireland (9), Italy (2), Malta (1), Multiple Countries (8), Netherlands (6), Poland (4), Romania (1), Spain (2), Switzerland (15) and United Kingdom (15).
Lead the development and execution of clinical pharmacology strategies for ground breaking small-molecule programs. In this pivotal role, you will directly influence key decision-making processes, support regulatory interactions, and help build a
Driving all aspects of purification process development, characterization, and technology transfer to cGMP manufacturing for hybrid and continuous processes; Serving as an internal technical resource for cGMP manufacturing and Process Design as well as a
Strategic and scientific leader within Clinical Development, driving the advancement of ProQR’s pipeline and contributing to improved patient outcomes. As a subject matter expert in CNS diseases, the Medical Director provides deep scientific and
In this position, you will be responsible for driving developability activities to support early and late-stage projects, with a strong focus on risk assessment and data-based decision making. You will lead and develop a small team of research analysts
This person will join a fast-paced, collaborative, and multidisciplinary team to support purification process development at the bench and pilot scale for the advancement of low-cost biotherapeutics manufacturing. Experience with high throughput
Responsible for leading and managing pharmaceutical development projects of drug entities within Development Bioanalytics (DevBA) from various customers and in different pre-clinical development phases; Accountable
Use all imaginable chemistry tools and methods to develop and optimize commercial process for selected drug substance route (photochemistry, biocatalysis, flow chemistry, electrochemistry, on-line analysis/PAT, high-throughput experimentation, structural
This individual will lead the organization to develop industry-leading analytical methods, analytical characterization packages, and control strategies to advance the manufacturing, conjugation, formulation, and process development for
Your mission is to ensure the smooth execution of strategically aligned research projects, drive scientific and technical excellence across the group, and support the continuous development of the Group Science & Technology. You will act as a key
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
You will provide technical leadership and scientific expertise to support the commercial manufacturing of pharmaceutical products. This role is responsible for ensuring robust process performance, driving continuous improvement, troubleshooting technical
The successful candidate will lead a Biologics Engineering team and oversee biologic projects primarily focused on Inflammation. The core responsibilities include biologics design and optimization to enable discovery projects from conceptualization to
Ensuring strategic support is provided to Global Project Team (GPT) assignments and wherever necessary, takes the lead in ensuring procedural documents relevant to GPT as applicable, to relevant GxPs and capture the right level of regulatory importance.
Responsible for both Chemistry and Microbiology Lab Assets, ensuring that the Lab is advanced in its technologies while ensuring compliance and best practices are adhered to. The role ensures efficient and innovative technologies and ideas are being
This role is accountable for the vision, direction, and performance of the Bioanalysis and Immunoanalysis/Immunogenicity groups, ensuring the delivery of high-quality, regulatory-compliant data for pharmacokinetics, pharmacodynamics, and immunogenicity
You will take a leading role in mRNA downstream process development, owning complex purification challenges from experimental design through data interpretation. You will work with a high level of independence, while collaborating closely with
Act as a subject matter expert (SME) for drug product (DP) manufacturing and validation activities; Lead and deliver MSAT projects focused on process optimization, robustness and cost improvements throughout the product lifecycle
He/She will support the QA program to assure the accuracy and quality of scientific data submitted to regulatory agencies in support of new drug applications and/or biological licensing agreement applications. The R&D QA Manager will collaborate and
Contribute to the design of novel and efficient synthetic pathways for drug substances undergoing clinical development; Conduct and oversee route scouting in laboratory to demonstrate synthetic viability; Use all imaginable chemistry tools and methods to
Support the execution of product changes in compliance with international regulations and quality standards; working with cross-functional teams and/or SMEs to ensure problem-solving, decision-making and change execution occur within project timelines.
Responsible for the development, maintenance and adherence to Genmab’s clinical data standards including eCRFs, edit checks, electronic case report forms (eCRFs) Completion Guidelines, controlled terminology, CDISC, CDASH and etc. The Associate Director
Provide epidemiology and statistical analytical support for RWE studies; Contribute to the development of evidence generation plans and design of RWE studies for scientific and regulatory purposes; Advise study teams on research methodologies and
Provision of scientific and technical leadership to multidisciplinary teams to achieve corporate goals in challenging research projects within early-stage biologics drug development. Establishing and managing research projects as project scientist;
You will utilize your analytical chemical expertise to work at the intersection of chemistry and biology. Your focus will be on defining, developing, and optimizing analytical chemical methods, defining clinically relevant extractions for chemical
You will play a key role in advancing Lonza’s Vector Engineering R&D capabilities, leading innovative scientific projects and developing people, while contributing hands-on expertise in recombinant protein production and mammalian cell culture.
Are you ready to lead cutting-edge analytical strategies for biologics? We’re looking for a Principal Analytical Scientist to drive method development, lifecycle management, and testing support for commercial products. This role is pivotal in
Manage a team of engineers, scientists and technicians in the development and implementation of new capsules, new capsules applications or related programs/projects in line with the R&D strategy and timelines; Define roadmap for the innovation
You will take on both strategic and operational responsibilities in advancing innovative therapies in autoimmune diseases, oncology, with a focus on advanced therapy medicinal products (ATMPs), including cell and gene therapies. In this role
Overseeing the overall end to end COE Research group covering pDNA, mRNA & Delivery (including Lipids discovery, associated synthesis) research teams and capabilities supporting Sanofi ambition in the field of therapeutic and prophylactic approaches
EuroScienceJobs is the best job board to find research and postdoc science jobs in Europe. Jobs in bioinformatics, biostatistics, biomedical research, biotechnology and genetics, microbiology and more. Research jobs across Europe including Belgium, France, Germany, Netherlands, Switzerland, UK and more.