QA & Ra Medical Devices

hace 4 días

Barcelona, España Page Personnel España A tiempo completo

This exciting position will give you the opportunity to work in a diverse international environment. You will be responsible for the quality system of our sales office in Barcelona as well as supporting in the registrations for Spain.

**KEY RESPONSIBILITIES & ROLE**
- To maintain the Quality Management System for our Spanish Organization
- Prepare and lead the quality management review meetings
- Training and coaching people on the procedures and processes
- Identify local regulatory requirements and lead impact assessment which is driving quality management system changes
- Execute Local regulatory registrations where necessary
- Supporting internal and external audits
- Leading clinical data collection for submission and PMCF
- EMEA regulatory affairs activities concerning importer and authorized representative requirements

Experience with quality processes in medical devices|3 years' experience in a QA& RA role
- Relevant Master of Science or bachelor's degree
- Experience with quality processes in medical devices
- At least 5 years' experience in a quality assurance or regulatory affairs role
- Advanced excel knowledge such as creating pivots and macro's
- Analytical skills
- Language skills: good written and verbal English and Spanish communications skills required
- Strong communication skills
- Passion for quality and to do things right

Our client is a global medical technology company that specializes in the development and sale of surgical products
- Barcelona city office
- **Great salary package**:

- Social Benefits
- International scope

A global medical technology company is looking for a QA & RA Medical Devices

QA & RA Medical Devices

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