Medical Device Regulatory Affairs Specialist
Regulatory Affairs Specialist
Our client is a developer and international supplier of blood component and cellular technologies. They need someone to offer support to their Regulatory team.
Principle Duties and Responsibilities:
Our client seeks a Regulatory Affairs Consultant from the Medical Device industry, with experience planning and writing Regulatory Submissions and PMAs, They are looking for someone that is familiar with Asia’ s regulations – APEC. This person will be helping with ECOs from a regulatory affairs standpoint.
- Medical Device (Class III): 5 years
- Regulatory Submissions: 5 years
Class III devices
Job Type: Contract