Release and Stability Coordination Officer

Job profile

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 will play an important role in a small and dedicated team named “Release & Stability Coordination”. You coordinate 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, shipments of samples to external labs and writing of stability study protocols and reports. Furthermore, you support the management of reference standards. A crucial part of your job is the maintenance and programming of a Laboratory Information Management System (LIMS).

You will be part of an experienced department named “Analytical Development and Quality Control”  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?

Ownership of activities 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. You are result-oriented and use proactivity and creativity as your methodology to find improvement opportunities. You are self-motivated which enables you to work with a high degree of independence and control.

• BSc degree in Biotechnology (HBO degree) or other relevant life science field
• At least 3 years of experience in a biopharmaceutical GMP environment
• An excellent quality mindset, curious attitude and eagerness to continuously improve processes
• Good knowledge of GMP regulations within the biopharmaceutical industry
• Experience with pharmaceutical IT applications such as LIMS is a strong preference
• Experience with project management is a strong preference
• Demonstrated good writing skills in English
• Excellent communication skills
• Team player
• A can-do attitude, hands-on mentality embracing cross-functional collaboration

Benefits and well being

Besides a competitive salary, we offer you a dynamic working environment at our state of the art campus in Nijmegen. Our values as integrity, authenticity, entrepreneurship, quality and trust are very highly regarded. We also offer an excellent pension scheme, 30 days annual holidays based on a fulltime position and we organize several company events throughout the year.

Join Byondis and create the future you want, today

Contract hours: 32-40 hrs/week, preferably fulltime

Salary: depending on experience

Location: Nijmegen

If you are interested in joining Byondis in this challenging position, we welcome your application via the apply button.