Location: Munich
Salary: Negotiable
Discipline: Medical Devices
We have an exciting opportunity for a Vice President to join an established leader in the medical device market, with the company operating globally.
Key Responsibilities:
Managing activities related to medical device compliance
Perform activities that align with ISO 13485, EU MDR (2017/745), FDA - 510k, MDSAP
Carry out training for staff on all policies for working in an environment that is regulated
Oversee CAPA activities and audits
Manage and submit information for databases
Serve on committees including the global regulatory board
Key Requirements:
Science degree (BSc)
8+ years in regulatory affairs (medical devices)
Understanding of ISO 13485, MDSAP and MDR
Ability to work in a cross-functional team and also independently
Ability to travel frequently nationally and internationally
Positive attitude
