Clinical, Quality and regulatory affairs manager.

Responsibilities
1. Take part in the regulatory strategy definition
2. Implement quality SOPs in the company
3. Assist with QA on-going tasks
4. Take charge of the planning and execution of the clinical studies
5. Prepare regulatory file submission
6. Establish a Scientific Advisory Board
7. Manage work with consultants
Qualifications
1. A minimum of 5 years of practical experience
2. Experience with regulation processes of medical devices
3. Bachelor’s Degree – life sciences preferred
4. Native English speaker
Personal skills
1. Independency – initiative, resourcefulness and proactive state of mind
2. Excellent communication skills and strong collaborative approach
3. Execution and service orientation
4. Organized
5. Fun ☺