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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...
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...
Design and lead innovative research projects that address key scientific questions; Develop international grant proposals and lead collaborative research programs...
You are responsible for leading and coordinating the outsourcing of drug substance development and manufacturing activities. This critical role ensures optimal supplier...
Ensure regular Quality interaction with other Departments including Validation, Manufacturing, Quality Control and Maintenance and represent QA Manufacturing as Risk Champion....
Primary activities will focus on Medical Monitoring Delivery & PV Support. The medical monitor will independently deliver all medical support required for successful delivery of...
They will lead the Chemistry, Manufacturing and Controls (CMC) organization, encompassing Analytical Chemistry and Formulations, while working cross functionally with Regulatory...
Provides global regulatory leadership of assigned program(s); Develops global regulatory strategies, including risk assessment and mitigation strategies; Participates in strategic...
Are you passionate about pushing the boundaries of biotechnology? Do you thrive in a cutting-edge environment where your work directly impacts the future of medicine? If so, Lonza...
Optimize nonclinical development plans for products. Collaborate with project/asset teams to deliver optimized development plans. Handle non-clinical drug safety aspects in various...
Play a key role in executing Medical Affairs Evidence Generation projects for both approved and pipeline products. This position will be responsible for overseeing a molecule...
Leads a team of Group Heads and Scientists. Ensures process development stages for liquid and lyophilized parenteral drug products (DP) of biologics (e.g. monoclonal antibodies,...
This role will be responsible for provision of analytical methods, data and information using analytical techniques in supporting site manufacturing processes and network projects...
You will be responsible to develop & maintain the strategy of Global Quality with respect to Analytical Technology and harmonization by leading the Global Analytical Science and...
ProQR is looking for an allround nonclinical subject matter expert who will be responsible for the design and monitoring in vivo studies (through selected vendors), evaluation of...
You will lead multiple pharmaceutical development projects to ensure effective collaboration between internal & external stakeholders to meet the objectives of Hovione and our...
Planning, performing and interpreting metabolite profiling studies up to and including human ADME studies for regulatory submissions, including MIST evaluation. This will be...
You will lead research programs in collaboration with internal and external partners focused on the development of novel drug candidates for the treatment of chronic liver...
Independently design, perform and analyze in vitro experiments to generate impactful data to support our pre-clinical assets such as small molecules, biologics or RNA-modulating...
Lead and manage a team of scientists and technicians to conduct bioassay, ELISA and SPR experiments in support of biosimilar development programs...
Review and analyze data from clinical trials, post-marketing and other relevant sources for the prompt identification of safety signals. Review and evaluate serious adverse event...
In this role, you will contribute to the characterization of biopharmaceutical molecules, supporting client projects through advanced analytical techniques. Perform LC-MS analyses...
This position is a scientific and strategic position in the DMPK department which is a part of Early Clinical Development -Translational Science (ECD-TS) group in the Patient...
Conduct protein analysis with emphasis of their physical and chemical properties, e.g protein impurities evaluation, glycosylation, molecular mass, amino acid composition etc...
Design, plan, perform and document scientific experiments as well as analyze and interpret the results to drive development and validation of analytical methods for simple and...