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The manager will lead and develop the team as well as providing mentoring, support and professional development to individual members of the Medical Writing Team. In addition, the...
You will be responsible for in-house GLP/GCLP infrastructure, systems and procedures to ensure adequate rigorous laboratory practices & regulatory requirements for analytical...
As a senior global regulatory lead, you will be responsible for our gene therapy project's regulatory activities and strategies focused on treating severe cancer diseases...
The GMS project manager leads the coordination/orchestration and execution of all aspects of assigned projects, including Launch, Lifecycle, and Divestment. She/he is accountable...
To excel in the role of our new Director - Global Launch Lead, your primary responsibility will be overseeing the launch of one of our products. This entails leading a...
The Head of R&D QIAGEN Gdansk will be responsible for all R&D related activities in our Center of Excellence for Enzymes & Proteins in our Facility in Gdansk, which is specialized...
The Senior Clinical Trial Manager (CTM) serves as the clinical functional lead, accountable for the clinical monitoring/site management delivery of assigned tasks and project(s) as...
Be key account manager for CMOs for labeling and packaging activities of final drug product, transfer to and storage at drug depot, as well as for distribution logistics from drug...
Provide internal and external medical support for the Oncology portfolio by being an expert on products, patient treatment trends and scientific activities within the disease area,...
Provide SME expertise to perform process characterization of the related pharmaceutical processes to increase robustness and sustainability. Review the sterile site aseptic...
In this role, you will be working on projects that create CHO cell lines and gene expression platforms with enhanced performance characteristics. You will be working within a team...
As our new Director, Global PV Operations you will become responsible for PV Operations activities and provide strategic and operational PV/quality/safety support for Ascendis...
The main objectives of the Program Lead are to lead the design, development, industrialization, and life cycle management of medical device programs for UCB’s medicines. The work...
Embedding operational excellence principles and mindset across all processes and personnel, you will also be responsible for the analysis, review and release of raw materials, bulk...
Contribute to Global brand strategy and development ideas, including optimisation of brand, global positioning, global messaging, and execution of global marketing strategy and...
The scientist in these roles should act as a local expert for developing assays to support projects, from target validation through to lead optimisation. The scientist in this role...
Responsibilities include the implementation of outcomes research strategies, health economics research planning, and process improvements to ensure patient access to Daiichi...
You will ensure seamless management of clinical projects; You will be responsible for the planning and executing of clinical trials in phases 1-4 within all of Ferring’s...
You will contribute to clinical study reports, data analysis review, publications, and study strategic development; You will lead the trial team with representation from relevant...
Conceptual design of pharmaceutical development studies for liquid and lyophilized parenteral drug products of large molecule biologics, peptides, vaccines and small molecules...
As a Regulatory Affairs Manager you will be responsible and accountable for all local operational aspects of regulatory submissions providing planning and technical support for...
Having responsibility of reviewing, assessing, recording and reporting of investigations of deviations occurred during manufacturing and testing of medicinal products, medical...
Oversees development and implementation of worldwide regulatory strategies for projects and issues affecting new product or new indication development; Leads interactions and...
The Senior Director Medical Excellence is responsible for maintaining and further develop a medical excellence platform supporting all Sobi therapeutic areas aiming to further...
Are you ready to play a role in public health protection and contribute to the quality of medicines worldwide? Do you think you have the right mix of scientific, relationship...
Samen met de CFO en de CEO/DGA vorm je het directieteam waarbij je rapporteert aan de CEO. In deze uitdagende directiepositie ga jij een belangrijke bijdrage leveren aan de...
Implement and develop new processes and optimise drug substance scale up activities. Play a vital role in contributing and delivering pharmaceutical APIs. Use of chemical knowledge...
Lead the development and implementation of the site R&D strategy including alignment with the site objectives and Global R&D; Responsibility for leading the development, scale-up,...
Act as a specialist in the area of oncology. Represent Regulatory Affairs internally working on a collaborative basis both within Europe and globally as a member of a...
You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics...
Leads the Immunogenicity and Ligand Binding Assays team and the design and execution of phase-appropriate clinical bioanalytical strategies, including quantitation of therapeutic...
Guarantees cGMP compliance in all activities and systems related to Projects and Products execution. Assures that working practices are streamlined and aligned with the actual...
The main purpose of this position is establishing and maintaining a domestic Pharmacovigilance (PV) unit, being responsible for carrying out all PV activities as described in...
This position of R&D Manager is a member of our global Hard Capsules R&D team in charge of developing new and optimizing existing products. The post offers a very...
he Senior Manager of R&D Quality will proactively promote compliance to Good Clinical Practice (GCP) regulations by providing Clinical and Research Development teams compliance...
The Clinical Trial Supply Manager (CTSM) represents product supply in the Clinical Study Teams and drives the development and execution of effective product supply strategies in...
The Sr. Manager Medical Affairs Oncology Medical Spain & Portugal is responsible for supporting the development and execution of the national medical strategy and programs that...
Avantor is looking for an organized and customer-focused R&D Manager to join the EU North Hichrom R&D team, developing projects that support the pipeline of new products and...
The Associate Medical Director Clinical Science Haemophilia is responsible for Sobi’s clinical development activities for one or more product(s)/indication(s) in the therapeutic...
Providing Clinical Devices Quality input to cross functional teams dealing with complex and important projects and issues. Providing mentoring and guidance to other members of the...
Provide medical expertise in support of company molecular biology and sequencing-based initiatives, as well as “big data” and large analytics projects. Provide oversight and...
Responsible for execution for medicinal products supervised designing CMC strategies and providing guidance to ensure regulatory compliance in time and quality; Set up, review and...
Drive formulation development process for drug type of project, new products, switches, line extension and business protection for the main Brands of CHC portfolio; Support...
Develop and validate new processes and control paradigms in ambr250 workflows; Develop small scale model, and scale down models using high through put systems, such as the ambr250...
Performing Data Management of Clinical Safety & Pharmacovigilance (CSPV) information of ICSR from clinical trials and marketed products. Ensure regional ICSR team compliance with...
Deviation and CAPAs management, including investigation, closure coordination, and partnering with end users to drive understanding and compliance to the QMS; Operationally...
As a key member of the analytical group, the successful candidate will have significant experience in immunoassay, cell-based assay and qPCR method development and...
Develop and manage a complete marketing program for the successful introduction, marketing and sales of products in the assigned territory. Continuously review and analyze sales...
The Director, Global Oncology Medical Affairs, Evidence Generation role is responsible for co-leading a crossfunctional Evidence Generation Team and developing an Integrated...
As our new Associate Director RA Device, you will be driving the regulatory strategy for device constituent parts of combination products and use your device regulatory experience...
The Associate Director Medical Affairs, CEEI will be responsible for the medical strategy of all business segments (MPT, HST, Pharmaceuticals) within the cluster and will oversee...
Collaborate with and provide global support for all R&D sites as part of a newly formed global CMC management organisation on small-molecule API development projects from...
Support the Medical Leadership in implementing medical strategy applicable to assigned therapeutic area; Develop and deliver an annual medical clinical plan in line with the...
Implement robust workflows for sample preparation, LC-MS-based omics, high throughput liquid chromatography, MS acquisition, novel data analysis approaches, and quantitative data...
As a Senior Scientist you will join the Characterisation team within Development Services at our site in Slough, you will be responsible for the planning and execution of...
The position manages end-to-end delivery of data management services for assigned projects/studies, collaborating with CROs and other vendors to ensure high quality deliverables...
Participate in development of novel methodologies for spatial lipidomics, metabolomics and proteomics; Performing routine tasks competently and independently, and generate reliable...
The Senior Director, Global Oncology Medical Affairs is responsible for developing the Global Medical Affairs (GMA) strategy and tactical plan as part of the Global Brand Strategic...
You will lead, mentor and manage the team using your experience in protein sequence and structural analysis along with a strong understanding of molecular interactions to deliver...