24.04.24 | Vollzeit | Augsburg | Daiichi Sankyo Europe GmbHTo ensure incidents and change requests are managed and addressed in appropriate timely manner Act as the point of escalation for the stakeholder and escalate internally and externally where necessary Report KPI´s and SLA achievement and manage violations or major service issues. Act as escalation instance
Später ansehen24.04.24 | Vollzeit | Pfaffenhofen an der Ilm | Daiichi Sankyo Europe GmbHManager executes our strategic stakeholder management programs and projects on a European and national level with the focus on our cardiovascular portfolio and our production site in Pfaffenhofen, near Munich. The candidate should have extensive experience in Policy and Public Affairs with a particular
Später ansehen24.04.24 | Vollzeit | München | Daiichi Sankyo Europe GmbHCreating novel therapies for people with cancer. Our European headquarters are in Munich, Germany, and we have affiliates in 13 European countries and Canada. We are seeking highly qualified candidates to fill the position European Health Economics Outcomes Research & Real World Evidence Senior Manager
Später ansehen24.04.24 | Vollzeit | Augsburg | Daiichi Sankyo Europe GmbHTo ensure incidents and change requests are managed and addressed in appropriate timely manner Act as the point of escalation for the stakeholder and escalate internally and externally where necessary Report KPI´s and SLA achievement and manage violations or major service issues. Act as escalation instance
Später ansehen24.04.24 | Vollzeit | München | CatalYm GmbHAnd external quality-related issues Support and processing of inquiries and qualification questionnaires as well as contracts Who you are Completed scientific/medical/pharmaceutical studies or training as an MTA/PTA or similar 3-5 years of experience in quality management in a GCP-regulated environment
Später ansehen24.04.24 | Vollzeit | Planegg | CatalYm GmbHAnd external quality-related issues Support and processing of inquiries and qualification questionnaires as well as contracts Who you are Completed scientific/medical/pharmaceutical studies or training as an MTA/PTA or similar 3-5 years of experience in quality management in a GCP-regulated environment
Später ansehen24.04.24 | Vollzeit | Oranienburg | Takeda PharmaceuticalIn the change management team, you can expect varied and challenging projects along the way from day one entire value chain of pharmaceutical production. Your main responsibilities Deploying AGILE program across sites and functions in order to build expertise and common understanding of the program. Ensuring
Später ansehen24.04.24 | Vollzeit | Frankfurt am Main | BioNTech SEExperience in quality assurance, quality oversight, project management or relevant experience, ideally in a biotech or pharmaceutical company Good combination of strategic skills; ability to make profound decisions in a highly dynamic and flexible environment Quality mindset and profound knowledge of EU GMP
Später ansehen24.04.24 | Vollzeit | München | Daiichi Sankyo Europe GmbHThe position holder will manage, with direction, end-to-end delivery of Statistical Programming ser-vices for assigned studies, collaborating with CROs and other vendors to ensure high quality deliverables are on time and within budget. The position holder will partner with internal and external stakeholders
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