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This position will oversee purification development for both early and late stage processes including process development, optimization, characterization and technology transfer to...
The activities of your team will concentrate on the identification of novel therapeutic concepts in immune regulation and tolerance with the potential to lead to transformative...
Perform qualitative and quantitative analyses of compounds, including drug substances, drug product intermediates and drug product; Recommend the analytical characterization...
You lead a team of research associates and scientists dedicated to developing and validating (bio)assays for release and stability testing of antibody products. You will focus on...
Lead Scientific Strategy: Direct the scientific strategy for the project within Global Antigen Design, operating within a fast-paced and agile environment to drive innovation and...
Performing a range of analytical experiments using different separation and characterisation methods (IEC, SEC, RP, HIC, HILIC, CE-SDS, LC-MS and LC-MS/MS); Experience in...
You will be responsible for the development and optimization of the manufacturing processes from synthesis to the final API in collaboration with our customers as well as internal...
You will be key in leading a team (10-15 HC) of highly talented scientists and researchers in a matrix organization. You will shape, support, develop and optimize the team...
Write and review clinical (and nonclinical) documents for regulatory submissions in the EU and US, such as Module 2.5, 2.7, 2.4, 2.6, integrated summaries of efficacy/safety...
Provision of scientific and technical leadership to multidisciplinary teams to achieve corporate goals for challenging research projects within biologics early drug development...
This pivotal role is responsible for delivering an effective testing and analytical service to ensure that our plant's products consistently meet specified standards. As an...
Lead the teams of ESO Quality Assurance Managers, the Sandoz New Product Supply & Launch (NPS&L) QA team, and the ESO EU Release hubs in various locations around the globe within...
Lead and mentor a team of Analytical Subject Matter Experts for both biologics and small molecule drug products fostering innovation and technical excellence; Support the...
You will be responsible for the comprehensive execution and oversight of the Product Development Process (PDP) for a given project within our R&D group. In the role, you will drive...
This role is pivotal in driving biomarker strategies, early clinical development plans, and providing scientific expertise and strategic guidance. The successful candidate will...
Lead and provide technical expertise in the planning and execution of IVD assay development projects, acting as a knowledge expert for quantitative PCR (qPCR) diagnostic systems...
Responsible for the planning and organization of formulation and process development of various modalities - with a focus on parenteral formulation containing nanoparticular...
As a successful candidate, you will take the role of Team Leader In vitro Laboratory a team of 2-4 scientists engaged in drug discovery projects for biotech and pharma companies...
Lead and conduct research to develop and evaluate mRNA-based vaccines against infectious pathogens with a focus on optimizing vaccine performance and longevity of responses...
Responsible for supporting the overall CMC strategies within projects, and manage project teams for the development of small molecule pharmaceuticals. Accountability to lead teams...
This position allows you to lead and execute process optimization projects, driving improvements in manufacturing process performance and efficiency. By utilizing your scientific...
The Tech Management Lead Drug Product is responsible for the management of technology transfer of the manufacturing processes of solid and/or parenteral Drug Products for...
You will play a critical role in all aspects of ADME (absorption, distribution, metabolism and excretion) covering multiple modalities across drug discovery and development. You...
Ensure compilation, submission and approval of CTAs and INDs for all clinical trial-related regulatory activities, maintaining these throughout the development phases. Provide...