QA Officer

Byondis is an independent Dutch biopharmaceutical company, based in Nijmegen, that focuses on developing innovative medicines against cancer and autoimmune diseases. We are driven by one goal: to develop new treatments to improve the standard of care for patients.

Your Role

Are you a Quality Assurance professional who wants to work in collaborative team in which you can grow and develop your skills?

You will join our Quality Assurance team, where you will contribute to maintaining a robust and compliant quality system that supports the development and manufacture of our innovative clinical products. As QA Officer, you will be responsible for vendor qualification and ongoing vendor management, ensuring that external partners meet applicable quality and GMP requirements. The role combines vendor management with the management and maintenance of training documentation, ensuring that relevant training records remain accurate and up to date.

What do you need to succeed in this role?

A quality mindset and the capacity to consistently deliver your tasks in a dynamic environment for First in Human clinical GMP production. Your are a team player taking responsibility for your own work which will strengthen our team. An open personality with good collaboration and communication skills. You are accurate, result-oriented and dependable. You are self-motivated which enables you to work with a high degree of independence.

• Bachelor in biotechnology related studies, life sciences or equivalent
• You have experience in quality assurance or other quality environment, or show a clear ambition to succeed in a quality role
• You have knowledge of the principles of cGMP or similar quality systems
• You demonstrate attention to detail in execution of your tasks and have affinity with computerized systems.
• You take responsibility for your tasks and deliver on time
• A can-do attitude, hands-on mentality and embracing cross functional collaboration
• You have excellent social skills, good communication in English and preferably Dutch and possess a collaborative approach

Why Join Byondis?

• State-of-the-Art Technology & Facilities: Work on a campus built for cutting-edge R&D, featuring our own in-house GMP manufacturing capabilities for ADCs and mAbs. Our focus on innovation means you’ll be surrounded by the latest in biopharmaceutical technology.
• Impactful Mission: Be a part of developing next-generation therapies that could redefine the standard of care for cancer and autoimmune diseases. Your QA expertise will directly influence the safety and efficacy of treatments entering first-in-human clinical studies.
• Collaborative Culture: Join a team where integrity, authenticity, entrepreneurship, quality, and trust create a dynamic, supportive environment for scientific advancement.
• Professional Growth: Expand your expertise in QA, gain exposure to a wide range of biopharmaceutical processes, and grow within a company committed to ongoing learning and development.
• Competitive Benefits: Enjoy a comprehensive compensation package, including a pension scheme, 30 days of annual leave (full-time), and a variety of company events to foster team spirit.

Join Byondis and create the future you want, today

• Contract hours: 32-40 hrs/week, preferably fulltime
• Salary: depending on experience
• Location: Nijmegen

Applicants must be nationals of a Member State of the European Union or hold a valid work permit for the European Union 

For further information, please contact Human Resources at tel. +31 (0)24 679 5100 or by email; recruitment@byondis.com. If you are interested in joining Byondis in this challenging position, we welcome your application via the apply button. Please send in your application before October 31, 2026.

Acquisition by any commercial agencies will not be appreciated.