As a successful, growing biotechnology company located in Amsterdam, the Netherlands, we offer a young, dynamic, and multi-national working environment. If you are passionate about providing the world with simple and affordable solutions to detect genetic aberrations, and enjoy a vibrant, family-friendly work environment: come join our team!
Find the position that is right for you.
We hire creative, inquisitive, and driven individuals for things like research, product development, bioinformatics, customer support, and quality control positions.
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As a bioinformatics Scientist you have an expertise in bioinformatics and an understanding of the cancer genome to identify cancer driver aberrations and to associate those genetic events with a diagnostic value. You develop new data analysis strategies for tumour analysis with MLPA. You are also involved in designing and testing MLPA products, so that they meet our quality standards.
MRC Holland is looking for a C# Developer in a young and dynamic biotechnology company based in Amsterdam–De Baarsjes. Our genetic tests are sold in more than 80 countries for hereditary and tumour research (www.mrcholland.com). Due to our continuous growth, we are looking for an Intermediate/Senior C# Programmer.
Are you an experienced C# programmer who wants to work on products that make a difference in a patient's life? Then we are looking for you!
As Quality Assurance (QA) Officer, you are responsible for the development, implementation, coordination, monitoring and management of one or more specific QA processes of the quality assurance system. You will also provide advice and guidance to MRC Holland staff concerning quality assurance systems and their implementation. You are part of the QA team and report directly to the QA Manager.
As MRC Holland’s Regulatory Affairs Specialist, you assist in ensuring that MRC Holland and its products meet regulatory requirements for its target markets in a swift manner that is compatible with other MRC objectives. This function requires understanding of the regulatory requirements applicable to In Vitro Diagnostics and Research Use Only products in the target markets. The Regulatory Affairs Specialist assists in the submission of registration files to relevant competent authorities and / or Notified Bodies, and collaborates with QA, Product Development and Technical Support departments to achieve departmental goals. You report directly to the RA Manager.
As a Junior Product Developer – Oncogenetics you already have some experience with, or strong affinity for, cancer genetics and an understanding of the cancer genome to identify driver alterations and to associate those genetic events with a diagnostic value. You are involved in designing and testing of (digital)MLPA products, so that they meet our quality standards. In addition, you are involved in developing and testing new data analysis strategies for tumour analysis with (digital)MLPA.
As a Junior Product Developer – Cytogenetics you already have some experience with, or strong affinity for, cytogenetics and epigenetics. You are involved in designing and testing of (digital)MLPA products, so that they meet our quality standards.
As a Project Leader Product Development, you will help transfer MLPA products from research use only (RUO) to in vitro diagnostics (IVD) status, to guarantee that our products can safely be used to diagnose patients.