Regulatory Affairs Project Manager EMEA Job Description
This role is responsible for leading and directing complex projects within the Central RA team. As part of the CEOT & EAR function, you will be accountable for ensuring compliance to European Medical Device Regulations (MDR) for Stryker products.
The key responsibilities include:
* Reviewing technical documentation against EU MDR requirements
* Working with international manufacturing sites to resolve issues
* Escalating regulatory compliance gaps and potential patient safety issues in a timely manner