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 Technical Documentation & Regulatory Compliance Specialist Long-term secure contract. International Project with top technologies Possibility of working remotely with a versátil schedule. Integration in a highly qualified team of professionals. Travel abroad with your project. Specialized training and continuous professional development. Social benefits and flexible compensation plan. Support the execution of regulatory and technical gap analyses between current documentation and NMPA requirements. Coordinate documentation activities across engineering, quality, regulatory affairs and external stakeholders. Ensure consistency across product specifications, design history files,



risk management documentation and quality records. Degree in Engineering, Life Sciences, Medical Technology or a comparable discipline. Experience working in regulated industries, preferably Medical Devices, Diagnostics or Life Sciences. Experience with Design History Files (DHF), Technical Documentation, Design Control and Risk Management documentation. Ability to work in cross-functional and international project environments. Experience with international registration projects. Knowledge of requirements traceability, document control and quality management systems. All positions require a high level of English (at least B2)
- please send your detailed CV in English.

📌 Technical Documentation (España)
🏢 ALTEN Delivery Centre Spain
📍 España