QA Officer

Byondis BV; Nijmegen; On-site; EUR 60,000 - 75,000; Full time

Benefits offered by this job

Pension scheme

30 days annual leave (full-time)

Company events

Job summary

Byondis BV in Nijmegen, the Netherlands, seeks a QA Officer to support vendor qualification and uphold GMP-compliant processes for first-in-human clinical production. You will manage external partners and ensure training records are accurate, collaborating with cross-functional teams to strengthen the quality system.

The role offers growth in QA, quality systems, and regulatory readiness within a collaborative biopharmaceutical environment.

Qualifications

• Quality mindset and collaborative spirit in a dynamic clinical GMP setting.
• Ability to deliver tasks accurately and on time in a First in Human production environment.
• Good English communication; Dutch language is preferred.

Responsibilities

• Vendor qualification and ongoing vendor management to ensure GMP compliance.
• Maintain training documentation and ensure accuracy of training records.
• Support the robust quality system across development and manufacturing activities.

Skills

Quality mindset

Team player

Attention to detail

Can-do attitude

Excellent communication

Cross-functional collaboration

Independent work

Education

Bachelor in biotechnology related studies, life sciences or equivalent

Tools

Computerized systems

Job description

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

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