QC Analyst potency assays

Nijmegen (Stad), Gelderland
Depending on experience
Closing date
7 Oct 2020

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Quality, QC Analyst
Full Time
Contract Type
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Job profile

The QC bioassay group consist of eight dedicated team members and is part of the Analytical Development & Quality Control department. Working at Byondis’ state-of-the-art facilities, the QC bioassay group supports the (clinical) development of our innovative medicines. As QC analyst you are responsible to execute, interpret and review potency assays, ensuring timely release of sample analysis requests. In this function you support the transfer and validation of these assays in close collaboration with the analytical development group. Good Documentation Practices and validated standard operating procedures are a prerequisite in our work.

As QC analyst for the bioassay group you enter observations and results into the appropriate trending databases for periodic analysis, trending, and troubleshooting exercises. You assist your QC team colleagues in maintaining proper overall operation of the department (physical inventories, logs, documentation, etc.), and with the implementation of quality improvement initiatives for QC laboratory operations. You also participate in laboratory, OOS, CAPA or other investigations

Your profile

  • A secondary or bachelor’s degree in Life Sciences, laboratory related field (Dutch MLO/HLO education or equivalent)
  • Demonstrated hands-on experience with cell culture and aseptic techniques, and cell-based and immunoassays
  • An understanding of cGMP regulations is a plus


  • Good verbal and written communication skills in English
  • A flexible and pragmatic approach, and able to work independently
  • Analytical mind, accurate, and ability to plan the workload
  • Team player
  • Ability to share thoughts, ideas and knowledge across in a constructive way

We are looking for an interactive team player to join our QC group, and who will effectively collaborate with colleagues from the bioassay analytical development group and physicochemical quality control departments.

Information and application

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

Contact information

For further information, please contact dr. Z. Kolen, Project Leader ADCQ, at tel. +31 (0)24 679 51 00. If you are interested in joining Byondis in this challenging position, we welcome your application via the apply button.

Important dates 

Please send your application before 28th September. The first round of interviews will take place on w/c 5th October, and the second round w/c 12th October.

Recruitment by commercial agencies in relation to this or other vacancies is not appreciated.



Around the world there are still people suffering from diseases for which no adequate medical treatment has been found.

For them we search, research and innovate in some of the world’s most advanced research facilities with the most talented people.

Byondis focuses on development of innovative medicines, including antibody-drug conjugates, in two key therapeutic areas: oncology and autoimmune diseases.

We provide a fair, human, open and inspiring working environment, with room for ambition, entrepreneurship and new initiatives - leading to innovative medicines with the potential to transform patients’ lives.

Byondis is based in Nijmegen, the Netherlands, where close to 350 staff work at our state-of-the art biotech campus.

  We are interested in result-oriented people with a sharp mind and entrepreneurial spirit, who can contribute to our ambition to provide solutions to the healthcare challenges of today and tomorrow.

Contact Us
  • Microweg 22
  • Nijmegen
  • 6545 CM
  • NL
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