Regulatory Affairs Manager (MDR) (m/f/d)

REFERENCE NUMBER:

411990/1

MY DUTIES:

-Monitoring of regulatory changes and introducing them into the company (e.g. MDR analysis and implementation)
-Implementing and leading EU MDR Task Force
-Performing of a gap analysis and creation of an action plan
-Provide global interpretation of MDR, provide harmonized recommendations to stakeholders
-Planning, coordination, preparation and submission of CMC variations and TypeII variations affecting the label via EU Centralized Procedure

MY QUALIFICATIONS:

-Solid knowledge of MDR
-Profound regulatory knowledge of EU Centralized Procedure for maintenance and development products
-Extensive knowledge of the biopharmaceutical products area in the EU

MY BENEFITS:

-An attractive remuneration package awaits you

PROJECT INFORMATION:

REMUNERATION DETAILS :

ABOUT HAYS:

With over 15 years of experience in the pharmaceutical industry, biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated professionals looking to develop themselves professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – all completely free of charge. Register with us and reap the benefits of job offers that are both interesting and relevant to your skills and experience.

MY CONTACT AT HAYS:

My contact person
Angela Akar

Reference number
411990/1

Contact
E-Mail: [email protected]