16.06.24 | Vollzeit | Berlin | ZEISSFor regulatory purposes (e.g. Clinical Evaluation Plan and Report, clinical content for regulatory submissions), including continuous gap analysis and conclusion on sufficiency of clinical evidence, adapt clinical strategy when necessary - Planning and execution of CA tasks of post-market surveillance incl
Später ansehen13.06.24 | Vollzeit | Heidenheim | PAUL HARTMANN AGEach other. - Provide and update documentation of clinical evaluation, post-market clinical follow-up and post-marketing surveillance - Cross-functional communication with other departments such as Marketing and R&D to ensure required input documentation is up to date - Coordinate external service
Später ansehen05.06.24 | Vollzeit | München | EPI Europrop International GmbHAnd good knowledge in engine production • 2-3 years (on-the job) experience, in supplier management, monitoring and surveillance • Good experience in various quality methods for investigations (8D, 5-Why, etc.) • Good knowledge in Aerospace regulations and standards EASA Part21/EN9100 • Good communication
Später ansehen05.06.24 | Vollzeit | München | EPI Europrop International GmbH• Report functional to the Supply Chain Manager and if requested to the Head of Product Delivery. Profile • Quality Engineer with aerospace background and good knowledge in engine production • 2-3 years (on-the job) experience, in supplier management, monitoring and surveillance • Good experience
Später ansehen07.06.24 | Vollzeit | Heidenheim | PAUL HARTMANN AGAnd/or experience in the areas of medical devices, technical documentation and regulatory product documentation, conformity assessment and post-market surveillance - Ideally a strong interest in and knowledge of electronic regulatory document control and management systems and associated processes - Open
Später ansehen24.05.24 | Vollzeit | München | JobLeads GmbH | 125.000 € - 150.000 € Physicians or scientists Accountable for all aspects of safety surveillance and risk management activities for assigned product portfolio (e.g. Oversees the development, maintenance of Safety monitoring plan, execute on safety monitoring activities including signal detection reports, signal assessment
Später ansehen21.05.24 | Vollzeit | Rosenheim | Daiichi Sankyo Europe GmbHWill be a product safety lead or part of a product safety team, and be responsible for overall product safety strategy or specific areas of safety surveillance and risk management, and provide safety leadership including but not limited to clinical studies, post-marketing surveillance, signal detection
Später ansehen21.05.24 | Vollzeit | Unterschleißheim | Daiichi Sankyo Europe GmbHWill be a product safety lead or part of a product safety team, and be responsible for overall product safety strategy or specific areas of safety surveillance and risk management, and provide safety leadership including but not limited to clinical studies, post-marketing surveillance, signal detection
Später ansehen21.05.24 | Vollzeit | Unterschleißheim | Daiichi Sankyo Europe GmbHWill be a product safety lead or part of a product safety team, and be responsible for overall product safety strategy or specific areas of safety surveillance and risk management, and provide safety leadership including but not limited to clinical studies, post-marketing surveillance, signal detection
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