R&D Quality Manager

Role Overview

The Quality Manager will manage complex projects and processes to support departmental portfolio, projects, and objectives according to agreed timelines and standards. They will ensure compliance with cGMP and regulations.

What You Will Do

Responsibilities include quality aspects of development projects and processes, quality problems and technical matters, release of medical devices, and representation in initiatives and cross-divisional projects.

Why It Might Be a Fit

The ideal candidate will have expert knowledge in Medical Device and Combination product regulations, project management skills, and excellent communication skills in English.

Requirements

• Expert knowledge in Medical Device and Combination product regulations (EU MDR, FDA CFR Part 820 and Part 4, ISO 13485)
• Functional Breadth - Quality Management, Change Control and Audit Management
• Project Management Skills - Critical Negotiations, Influencing Skills and Collaboration across boundaries
• Excellent communication skills in English

Benefits

• Competitive salary
• Annual bonus
• Pension scheme
• Health insurance
• 24 days annual leave
• Flexible working arrangements
• Employee recognition scheme
• Learning and development opportunities