On-site jobs in Austria (3), Belgium (10), Bulgaria (2), Croatia (5), Cyprus (2), Denmark (9), France (13), Germany (17), Greece (2), Hungary (1), Ireland (18), Italy (4), Lithuania (1), Multiple Countries (10), Netherlands (10), Poland (8), Portugal (8), Romania (4), Slovenia (1), Spain (5), Sweden (3), Switzerland (20) and United Kingdom (16).
This role serves as a close business partner and facilitator of regulatory activities and is expected to contribute to developing sound regulatory strategies globally. The role...
Lead the safety strategy of the assigned product(s) during clinical development including Company Sponsored studies, Investigator Sponsored studies, Compassionate Use and Disease...
You will play a pivotal role in ensuring the quality and compliance of Investigational Medicinal Products (IMPs) through your leadership and guidance of supplier management teams....
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...
Develops a strategy for external manufacturing of Teva’s products and manage its implementation, in collaboration with TGO leadership and commercial units. Establishes and...
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...
You will provide leadership for all Small Molecule QC laboratories related to Lonza’s Visp site. You will ensure adequate resources (staff, laboratory and instrumentation) to...
As part of our PV team you will be working collaboratively with the Global Product Safety Science Lead (GPSSL) for assigned product(s) as well as with other PV functions, to ensure...
Responsible for the planning and organization of formulation and process development of various modalities - with a focus on parenteral formulation containing nanoparticular...
Lead (Co-lead) the study teams to develop a cross-functional, integrated study implementation plan including creation of initial study budget, study kick-off and team meetings....
A managerial position responsible to ensure that assigned Quality Management System activities are managed in compliance with regulations and company policies and in accordance...
The core responsibility of the Medical Director is to lead the local medical department, be a part of pan-European R&D projects and work closely with other medical departments in...
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...
In this role, you will lead a team of five quality officers, providing direction and coaching to elevate both the quality of work and the motivation of your team. We are seeking a...
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...
Lead the planning and integration of Research and Development (R&D) activities at our pharmaceutical manufacturing site. Responsible for ensuring the efficient and effective...
This position allows you to lead and execute process optimization projects, driving improvements in manufacturing process performance and efficiency. By utilizing your scientific...
You will be responsible for overseeing all aspects of Quality for Research and Development of Aesthetic Filler products, including Design Controls, Risk Management, Design Changes...
Lead the Quality function team to perform batch review, testing and release activities to certify product in compliance with specifications and procedures, ensuring timely...
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...
You will oversee the execution of one or more clinical trials across different therapeutic areas and development stages, ensuring high-quality and timely deliverables. Participate...
Ensure compilation, submission and approval of CTAs and INDs for all clinical trial-related regulatory activities, maintaining these throughout the development phases. Provide...
Lead the safety profile of the assigned product(s) during clinical development including Company Sponsored studies, Investigator Sponsored studies, Compassionate Use and Disease...
You will lead and inspire a team of highly skilled managers, scientists, and technical professionals for supporting our mission of making cancer history. Your role is pivotal in...
Execute Early Access Program planning: Manage all aspects of EAPs, applying risk management principles; Coordinate with cross-functional teams: Align on strategic priorities...
This position is responsible for working with the physicians and other clinical scientists within Early Clinical Development to provide clinical research support for early phase...
The candidate will be responsible for overseeing all biochemistry/biophysics activities, managing a team of talented scientists. Provide in-depth biochemical/biophysical...
Formulate, lead and drive global CMC regulatory strategy for biosimilar projects/products drawing on substantial regulatory expertise with a focus on innovation, maximizing the...
In this role, you’ll be responsible for overseeing the scale-up of fermentation processes from lab to commercial scale, and you will be instrumental in leading our plant start-up...
You will manage PV staff and provide oversight to PV activities, workflow, processes, and procedures. You are also responsible for clinical PV (CPV) and post-marketing PV service...
You will manage uninterrupted supply of Gilead’s clinical and commercial products through execution of manufacturing campaigns within our global external contract manufacturing...
Design, plan, perform and document scientific experiments as well as analysis and interpretation of the results to drive development and validation of analytical methods for solid...