Are you looking for the next challenge in your career? Would you like to be part of an exciting highly qualified team of professionals in an international environment ? We are currently looking for a qualified Regulatory Affairs Specialist. Join an international division and work alongside with some of the most talented engineers and technicians from all over the world. Your benefi ts: Competitive Sal ary. Long-term secure contr act. International Project with top technolo gies Possibility of working remotely with a adaptable sched ule. Integration in a highly qualified team of profession als. Travel abroad with your proj ect. Specialized training and continuous professional developm ent. Social benefits and flexible compensation p lan. Responsibil ities: Support and manage regulatory activities related to the registration and approval of medical devices in China. Navigate and coordinate NMPA submission and approval pro cesses. Ensure compliance with Chinese regulatory requirements and applicable sta ndards.



Collaborate with cross-functional international teams, including Quality, Clinical, and Product Devel opment. Provide regulatory guidance and risk assessment throughout the project li fecycle R equirements Proven experience in Regulatory Affairs within the medical devi ce industry. Hands-on experience with NMPA regulations, submissions, and approva l processes. Strong understanding of the Chinese regulator y landscape. Experience with Class II and/or Class III medical devices is highl y preferred. Exposure to CGM, diabetes care, diagnostics, digital health, or wearable medical devices is a stron g advantage. Fluent Engli sh required. Chinese language skills are a strong plus. German is considered a nice-to-have We positively value all work or study exper ience abroad. All positions require a high level of English (at least B2) - please send your detailed C V in English.

📌 Regulatory Affairs Specialist. International Project. (España)
🏢 alten delivery centre in
📍 España