QM Associate – Product Registrations

📋 Description

• prepare regulatory submissions of medical devices to health authorities
• support local partners in the preparation of regulatory submissions
• monitor and implement laws and regulations that impact product registrations
• keep regulatory databases up-to-date
• support the maintenance and improvement of the product registration processes
• participate in and support internal and external quality audits

🎯 Requirements

• Degree in engineering or life sciences preferred
• Interest in quality management and regulatory affairs
• Knowledge of international regulations for medical devices is an advantage
• Ability to manage multiple projects
• Strong attention to detail
• Proficient in the use of MS Office

🎁 Benefits

• A mutually-supportive, international team
• Meaningful work with a lasting impact on medical technology
• 30 vacation days, plus December 24th and December 31st
• Flexible working hours as well as hybrid work model within Germany
• Bike leasing via cooperation partner 'BikeLeasing'
• Parking garage and safe underground bike storage