changes. Provide regulatory guidance and support to cross-functional teams, including R&D, Clinical Affairs, Quality... requirements and guidelines, including FDA regulations (21 CFR), ICH guidelines, and other applicable regulations. Experience...
, France Posting date: 21 Oct 2026 Reference: BBBH71149 Build trusted partnerships with surgeons, support life-changing... in the O.R. and during follow-up patient care as required. This position requires excellent relationship management, teamwork...
Lugar:
France | 23/10/2026 02:10:41 AM | Salario: S/. €85000 - 95000 per year | Empresa:
Proclinical with a pragmatic and entrepreneurial mindset. Regulatory affairs is closely integrated with R&D, commercial, and supply chain teams... 21 | Article 34 | Article 43 | Article 44 | Zonal Evaluation | Rapporteur Member State | RMS | ZRMS | Authority...
technologies and/or new clinical system technologies of interest for R&D. Develop, coach, and mentor team members;support... with AWS, R Shiny, AI/ML, Rave APIs, MySQL, Python, and Tableau. Familiarity with Electronic Data Capture Systems...
Posting Start Date: 9/21/26 At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through... submissions and the success of the Daiichi Sankyo R&D pipeline across therapeutic areas. The role partners with cross-functional...
Contexte et missions KARPOS RH is recruiting on behalf of one of its clients, an R&D center specialized in the... development of innovative medical devices and technologies in the healthcare sector, a R&D Project Manager - Medical Device...
Lugar:
Lyon | 03/09/2026 20:09:05 PM | Salario: S/. €50000 - 55000 per year | Empresa:
Karpos RHContexte et missions KARPOS RH is recruiting on behalf of one of its clients, an R&D center specializing in the... development of medical devices and innovative technologies in the healthcare sector, a R&D Project Manager - Peptide Development...
Lugar:
Lyon | 03/09/2026 19:09:30 PM | Salario: S/. €50000 - 55000 per year | Empresa:
Karpos RH 13485 and MDR 2017/745 Navigate the complexity of AI/software medical device regulation Act as a strategic partner to R... Review R&D deliverables and technical documentation Participate in risk management activities (ISO 14971) Ensure product...