We're sorry, the job you are looking for at Daiichi Sankyo Europe on EuroPharmaJobs has expired.
Click here to see more jobs at Daiichi Sankyo Europe .
We still have many live jobs. Click below for similar jobs in:
or go to our job search page.
Develop Manufacturing Industrial Strategic Supply Plans (ISSP) for products throughout their lifecycle; Build and maintain a portfolio of strategic projects related to...
ProQR is looking for a nonclinical subject matter expert with experience in GLP toxicology studies according to regulatory guidelines. The candidate will play an essential role in...
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...
Responsible for overall quality of AbbVie products which may include small molecule pharmaceuticals and/or biologics, combination products to ensure business objectives are met...
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...
Assist the development and implementation of immunological assays, such as ELISA, virus neutralization assays, ELISPOT, flow cytometry, etc., within the CEPI laboratory networks...
The candidate will serve as the bioanalytical lead for one of the argenx compounds, represent the bioanalytical team in one or multiple project teams, and closely collaborate with...
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...
You own your assigned projects, are responsible for the projects progress and ensures that everything required to make it happen is available and/or performed. You communicate with...
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...
You will possess strong skills in physico-chemical methods related to H/UPLC and CE method development and qualification, large molecule (mAbs) characterization, a mentoring team...
You will oversee batch release quality and compliance across internal sites and third-party maufacturers, ensuring all products (pharmaceutical and non-pharmaceutical products)...
You lead CMO vendor teams for daily operational management and coordinate meetings with UCB multifunctional teams; You participate in CMO selection for new and existing products,...
Co-ordinate experiments with CRO’s; Review, interpret and report data in support of drug discovery projects; Present data at multifunctional project teams; Work collaboratively...
He/she drives internal and external efforts with the aim of developing, producing and characterizing these therapeutics antibodies for early and late stage clinical programs up to...
You will oversee technical and business operations at designated external manufacturing sites, serving as the primary point of accountability for strategic and tactical activities...
She/He will lead the EMEA medical community providing medical guidance and expertise across organization and externally. Define the EMEA medical strategy in close collaboration...
Ensure regular Quality interaction with other Departments including Validation, Manufacturing, Quality Control and Maintenance and represent QA Manufacturing as Risk Champion....
You will participate in innovation projects as the quality representative, being accountable for the quality deliverables of the project. Thus, you will ensure product quality...
They will lead the Chemistry, Manufacturing and Controls (CMC) organization, encompassing Analytical Chemistry and Formulations, while working cross functionally with Regulatory...
Manage Clinical Safety activities and multiple large programs. Oversee clinical safety case management and aggregate reporting responsibilities to ensure client needs are fulfilled...
Owning all quality related responsibilities for the CQV Lifecycle Program for new facilities, equipment and utilities related to the GMP manufacturing of biologics & APIs;...
Developing the medical marketing content strategy of the brand; Effectively creating, managing, and executing educational and promotional marketing programs, and communicational...
Provide support to the reference standards team through the synthesis, purification and isolation of critical process and degradation impurities. Impurities will be synthesis to a...