QM Associate – Product Registrations (part-time 20h/week)

📋 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, but other degrees may be considered
• Interest in quality management and regulatory affairs
• Knowledge of international regulations for medical devices is an advantage
• Ability to manage multiple projects
• Very 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