Officer - Release and Stability Coordination team

Job Profile:

Officer - Release and Stability Coordination team

Byondis is at the forefront of innovative drug development, particularly in the field of oncology and autoimmune diseases, making impact on patients’ lives. Byondis offers opportunities for continuous learning and professional growth, making it an ideal place for those who are passionate about advancing their careers in the pharmaceutical industry.

You play an important role in a small and dedicated team named “Release & Stability Coordination”. This team coordinates the analytical testing that supports the release of production batches and associated stability studies. Your responsibilities include the management and distribution of analytical test samples and shipments of samples to external labs. Furthermore, you support the management of reference standards. A crucial part of your job is the coordination of the maintenance of our equipment (climate cabinets and freezers).

You will be part of an experienced department named ‘Analytical Development and Quality Control (ADQC)’  that performs both GMP and non-GMP activities within Byondis. To conduct your role effectively, you will have a continuous focus on accurate execution and improvement of (GMP) working processes and you will intensively collaborate with other departments, including Quality Assurance, Manufacturing Operations, Regulatory affairs, Supply Chain, Engineering & Maintenance, and IT.

What do you need to succeed:

You work proactive and result-oriented with a critical mindset on precision and quality of your own and your colleague's work. A natural team player with an attitude to collaborate and communicate, as well as being flexible to act in a fast changing and demanding environment.

• Degree in Biotechnology (MBO or HBO degree) or other relevant life science field
• An excellent quality mindset, curious attitude and eagerness to continuously improve processes
• Experience in a biopharmaceutical GMP environment is a strong preference
• Good knowledge of GMP regulations within the biopharmaceutical industry is a strong preference
• Demonstrated good writing skills in English
• Excellent communication skills
• Team player
• A hands-on team player with a ‘can-do’ mentality

What We Offer:
In addition to a competitive salary, we provide a dynamic work environment on our campus in Nijmegen. Our core values—integrity, authenticity, entrepreneurship, quality, and trust—are held in high regard. We also offer a solid pension plan, 30 vacation days per year based on full-time employment, and organize company events throughout the year.

Join Byondis today and create the future you envision:

• Contract hours: 32 - 40 hours per week, preferably full-time
• Salary: Depending on experience
• Location: Nijmegen

For more information, please contact Human Resources at +31 (0)24 679 5100 or via email at recruitment@byondis.com. If you are interested in taking on this exciting role at Byondis, please apply via the application button. Apply no later than January 31, 2025.

Acquisition by commercial agencies is not appreciated.