Byondis logo

Quality Assurance Officer

Byondis

Contractor
2-5 years experience
On-site

Key Skills

Vendor Qualification
Vendor Management
Quality Assurance
Good Manufacturing Practice
Current Good Manufacturing Practice
Quality Systems
Training Documentation Management
Training Records Management
Attention To Detail
Computerized Systems
Communication
Cross-Functional Collaboration
Time Management
Independence
English
Dutch

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 Location: Nijmegen Applicants MUST be nationals of a Member State of the European Union or hold a valid work permit for the European Union Acquisition by any commercial agencies will not be appreciated.

Core Responsibilities

Qualify and manage vendors to ensure external partners meet applicable quality and GMP requirements. Maintain training documentation and records, supporting a robust, compliant quality system for clinical product development and manufacturing.

Requirements

A bachelor’s degree in biotechnology-related studies, life sciences, or an equivalent field is required, along with experience in a quality environment or a clear ambition to pursue a quality role. Candidates should understand cGMP or similar quality systems and demonstrate accuracy, dependability, communication skills, and a collaborative, self-directed approach.

Benefits

  • Pension Scheme
  • 30 Days Of Annual Leave
  • Company Events

About Byondis

Industry: Pharmaceutical Manufacturing

Company size: 201-500 employees

Driven to improve patients’ lives, Byondis is an independent, fully integrated biopharmaceutical research and development company creating innovative targeted medicines for cancer. The company is developing new biological entities (NBEs) with a focus on antibody-drug conjugates. Byondis’ development portfolio leverages its expertise in linker-drug (LD) technology, antibody-drug conjugation and disease biology. Byondis’ fully integrated drug development capabilities cover all stages from pre-clinical and clinical R&D, production of clinical batches of the selected product candidates and regulatory filings, which are all done in-house. The company has a dedicated team of more than 200 staff working in its state-of-the-art R&D and GMP manufacturing facilities in Nijmegen, the Netherlands.

Added Today