26.04.24 | Vollzeit | Frankfurt am Main | Merz AestheticsPartner Management, Marketing, Medical Affairs, Regulatory, Commercial Excellence, Fiance, Sales) on various legal topics - Identifying training needs among business stakeholders and developing/ presenting training and education on relevant legal topics/ legal developments or use of existing templates
Später ansehen26.04.24 | Vollzeit | Frankfurt am Main | Merz AestheticsOr PhD - Approx. 3 -6 years of experience in international regulatory affairs field for medical devices - Experience in registration of high risk devices (class III) - Experience in medical device registration in Asia Pacific and Latin American countries - Fluency in Business English is a must - further
Später ansehen25.04.24 | Vollzeit | München | Bristol Myers SquibbExperience strongly preferred. - Pharmaceutical experience, including professional work experience in medical learning. - Has a strong knowledge of Medical Affairs' role & responsibilities, including field & office-based teams. - Knowledge of adult learning principles, learning design & executing learning
Später ansehen24.04.24 | Vollzeit | BIOMERIEUXCome and join a family-owned global company with a long-term vision, and a human-centered culture. We are looking for a Medical Scientific Liaison (m/w/d) Location Remote across Germany Reporting to the Cluster Medical Affairs Director and accountable of the IVD portfolio regarding Syndromic, AMR/AMS
Später ansehen20.04.24 | Vollzeit | Mainz | SCHOTT Pharma AG & Co. KGaATechnology) is required, and a PhD is preferred - You should possess 5-10 years of professional experience in regulatory affairs or medical devices, with a focus on interfaces with quality management. - Proven skills in project management and ability to think interdisciplinary. - Profound knowledge
Später ansehen09.04.24 | Vollzeit | Grasbrunn | TipTopJob Germany | Development and business growth. The Medical and Professional Affairs Director will be responsible for leading the Medical and Professional affairs strategy for Myopia, Presbyopia, Light Management, Clinical Optometry categories/Instruments, as well as eyewear solutions and their related products
Später ansehen27.04.24 | Vollzeit | Heidenheim | PAUL HARTMANN AGRegulatory affairs - Supporting the wider company in the maintenance and updating of documentation in accordance with relevant requirements - Ensuring product compliance to all relevant rules and guidelines Qualifications - Completed studies in natural science/engineering (e.g. medical technology, polymer
Später ansehen15.04.24 | Vollzeit | Biberach, Ingelheim am Rhein | Boehringer IngelheimHave an exciting opportunity for you to make a significant impact at Boehringer Ingelheim. We are seeking a dedicated professional to align our Global Regulatory Affairs (GRA) objectives across all functions, spearhead benchmarking efforts, and deliver valuable insights to refine our processes
Später ansehen14.04.24 | Vollzeit | München | ZEISSIn an international environment - You work very closely with content development managers, translation managers, linguistic asset managers, software developers, UX designers, marketing communication experts, regulatory affairs managers, and external partners to actively develop, standardize and align core terminology
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