Engaging, representing, being Black Swans 

Your Life Science Career Partner 

You want… 

A central role in the development of reliable medical devices and the registration of the products worldwide. By dividing your time between quality assurance and regulatory approval, you get the chance to work on several projects simultaneously in various ways and use your entire skillset rather than limiting yourself to only one area. 

You will… 

Develop strategies for regulatory approval, promote compliance of development activities, and support the registration process. Since you’ll be working on 1-3 projects at a time, you’ll have a lot of variation in your work and solve complex challenges, hopefully through a proactive mindset that comes naturally to you. 

You’ll join… 

A global leader of integrated end-to-end solutions of advanced drug delivery devices and connected health solutions whose employees are the heart and soul of the company. Focusing on long-term partnerships with their global clients, this company expects you to convert growth opportunities into successful wins for the organization. As part of the company, you’ll get the chance to work directly with competitive technology that makes life easier for patients and know that your contribution will improve and ease the lives of others. 

You have… 

• A bachelor’s degree in life sciences or engineering 
• Experience in quality assurance and/or regulatory affairs 
• Knowledge of MDR and ISO 13485 
• Experience working in a regulated environment, preferably in the medical device industry