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 (10), Cyprus (2), Denmark (2), France (7), Germany (6), Ireland (6), Italy (2), Multiple Countries (4), Netherlands (6), Poland (4), Spain (5), Switzerland (13) and United Kingdom (20).
You will lead and inspire a team of approximately 10 scientists (a mix of Research Engineers/PhDs and Technicians) dedicated to the design, optimization, and scale-up of synthetic processes for future drug candidates. Operating at the interface between
You will build and development of a team of multifunctional engineers to develop Orthopaedic instruments to support our Orthopaedic Instruments and Mako Robotic product Lines. This role will be a key leader in our Orthopaedic Instruments team,
Lead, coach, and develop Bioanalytical Study Management scientists as one integrated team, including goal setting, performance enablement, development planning, engagement, role clarity, and accountability for delivery; Set and drive the strategy for
You will be involved in the European Surveillance of Veterinary Antimicrobial Consumption (ESUAvet) activity, one of EMA's high-profile outputs supporting the fight against AMR. You will coordinate Member States’ data reporting contribute to data
Lead the design and execution of clinical pharmacology strategies and corresponding studies across multiple programs. Develop innovative and meaningful clinical pharmacology approaches that accelerate and de-risk drug development Define dose selection,
Develop and drive the nonclinical PKPD strategy for projects. Ensure translation from in vitro data and in vivo nonclinical studies to prediction of efficacy and safety in patients. Build PKPD models of sufficient complexity to allow hypothesis testing
Build and coordinate early-stage small-molecule discovery project teams, owning strategy, prioritization, and key go/no-go decisions - from hit finding to early lead optimization, towards valorization; Drive the integration of computational methods into
In this role, you will act as a subject matter expert within rare endocrinology and support the development and execution of global medical strategies across Ascendis Pharma’s growing portfolio. You will work closely with colleagues across Medical
You will lead the development and execution of global regulatory strategies in close collaboration with co-development partners and internal and external stakeholders. Acting as regulatory lead for complex projects, you will draw upon
Extrapolation (where appropriate), dose selection, trial design, PIP development and ongoing evaluation of data as generated. Transform PBPK and QSP analyses into actionable insights and communicate these findings effectively to project teams and
Lead technology transfers and regulatory submissions while managing multiple programs in line with CMC objectives and timelines. Apply Best Product at Pivotal and Speed to the Clinic principles, prioritize resources across competing programs, and ensure
Provide QA support and expertise to iPSC cell culture, cell banking, cell differentiation in bioreactor and aseptic manufacturing activities; Maintain a strong QA presence on the shop floor and promote a proactive, right-first-time quality culture;
In this role, you will serve as the primary scientific and operational lead for outsourced quantitative bioanalytical activities at Contract Research Organisations (CROs) ensuring high-quality assay execution, regulatory compliance
Design and execution of agreed work plans for the production and characterization of membrane proteins; Responsible for supporting multiple projects and may be asked to direct internal resources to achieve agreed goals
Utilize and establish advanced in vitro and in vivo models of ocular disease, and leverage available patient sample datasets to identify, validate, and characterize novel therapeutic drug targets; Independently lead and manage drug discovery projects from
Support the Drug Linker Development Organization Head in the ramp up phase of the Accelerate Asset Development unit by defining and supporting the implementation of all critical business processes for drug linker projects; Manage the hiring process of the
You will lead a new global organization consisting of groups based across multiple sites and countries and report directly to the Global Head of BioAnalytics, CMC Development. You will be responsible for analytical characterization of therapies across all
You will provide scientific leadership in interdisciplinary projects to elucidate structural mode of action and enable structure-based design with a focus on macromolecular complexes of antibodies, multispecifics and molecular degraders. You will
In this role, you’ll shape the future of our global biosimilar pipeline. You’ll sit at the crossroads of science, commercial strategy, and investment decisions - helping determine which biosimilar assets we invest in, when, and at what scale
Ensuring the sterility of injectable products through robust contamination control and sterility assurance strategies. This role extends beyond microbiological testing to encompass comprehensive oversight of aseptic manufacturing
Transfer, optimize, and develop bioanalytical methods to support product development and quality control. Plan, execute, and document method pre-validation studies in accordance with applicable regulatory requirements. Authoring of Standard Operating
Develop purification processes for active ingredients or intermediates ranging from the gram scale to several tens of kilograms (preparative liquid chromatography, batch, SFC, and SMB). Serve as the primary point of contact within your entity, ensure
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
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.