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Lead formulation development activities related to liquid and lyophilized parenteral drug products of large molecule biologics (e.g. monoclonal antibodies, novel formats, ADCs...
Ensure customer service level promises and logistics costs with the cluster VP & EMEA SC VP. In accordance with the Cluster Executive Committee, lead the Cluster Order Policy...
Responsible for Neuropsychiatry products launch activities, cross-functional leadership and management of Medical Science Liaisons (MSLs). You will represent medical affairs at...
This role acts as key Quality counterpart for growth projects and is responsible for leading quality activities by working closely with various quality and operational functions to...
The Vice President Medical Strategy and Head of the Hematology/Oncology COE provides strategic medical and scientific leadership, subject matter experience and expertise to IQVIA...
Ensure appropriate affiliate resourcing, skills and capabilities are in place to support affiliate, regional and global medical affairs activities, global research, and development...
Providing strategic counsel to clients on relevant health policy challenges and opportunities, and coordinating teams to deliver public affairs strategies; Leading client accounts...
You will lead the clinical development strategy and be responsible for designing and executing clinical development plans for MR Imaging assigned contrast agents...
You will provide therapeutic and drug development expertise and interact with Sponsors and investigative sites on protocol medical issues. Contribute to investigator meeting...
The candidate will contribute, with internal and external partners, to project proposals and innovative approaches in the field of antibody/biologics discovery to deliver high...
Develop and implement quality transformation strategies: You will be responsible for designing and implementing strategies to improve quality standards across the organization....
The Director Assay Development leads an international and multidisciplinary team of scientists and lab technicians who have their main focus on developing a completely new...
The successful candidate will be responsible for the in vitro cellular pharmacology function within the drug discovery team. You will use your extensive experience in people...
Develops, deploys and delivers OTC strategy aligned with global, Europe and International Market strategy; Defines focus and prioritize for investment in alignment with regions and...
The Head of Quality UK & Ireland will be responsible for the direct supervision of the company concerning all activities covered by the MHRA Establishment license and HPRA rules....
As the Director Protein and Cell Supply you will be responsible for the supply chain from vector design to protein production to logistics. You will lead three processes (and...
Rhythm is looking for a Sr Manager QA to play a key role in ensuring quality and regulation-based compliance during the manufacture and distribution of Rhythm clinical and...
Monitor and analyze the impact of emerging or revised laws, regulations, enforcement actions and other changes that impact the manner by which the clients' products are regulated...
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...
The candidate with be responsible for creating and maintaining Medical Affairs slide decks. The Medical Writer will collaborate with Medical Affairs stakeholders to create...
You will be responsible for leading global, complex extractables and leachables (E&L) projects with internal and external laboratories. You will work with site and global teams to...
Lead Global Med. Excellence and Stakeholder Engagement Team (Med. Communication, Med. Info, Capabilities and Learnings, Medical Service Hub, Medical Evidence Generation Management...
Your key responsibilities will be people management, coordinating screening workflows for projects at different discovery stages, and maintaining a versatile assay platform...
Responsible for managing GCP and GVP Quality Management Systems of Research and Development activities in accordance with applicable legal, regulatory and other Quality standard...
As an (Associate) Director, Global Regulatory Affairs Project Lead you will join our Global Regulatory Affairs organization. In this capacity, you will assume responsibility for...
Derives targets from a thorough assessment starting with biology and a deep understanding of genetics. Shapes the identification and prioritization of disease areas for the...