Scientist for quality control of cell products

Cell2Cure is looking for a scientist with experience in implementing, performing, and troubleshooting analytical methods for cell biology.

We expect you to have a high professional commitment, to be systematic, and meticulous, and to have an interest in GMP and analytical methods for cell biology.

Ideally you hold a master’s degree in health sciences or natural sciences, and years of practical experience with flowcytometry, ELISA, cell culture and GMP for clinical trials. General knowledge of regulatory requirements for analytical methods and advanced therapy will be an advantage.

We can offer you a working life where you can help make a difference for colleagues and patients alike. You will be part of a hectic but committed nnovative environment with a strong interdisciplinary collaboration. We guarantee you, that no two working days are the same.


Cell2Cure is a small Danish biopharmaceutical company that develops and produces investigational medicinal products based on stem cells isolated from adipose tissue. Today, our cell products are being tested in multiple clinical trials and diseases, nation-wide.

We are at the forefront of the development of clinical stem cell therapy. That requires drive and creativity and is rewarded with great responsibility and influence on solutions. You will be given an active role in a small group of dedicated entrepreneurs and developers, all with many different tasks, and the skills to pull together.

The job

You will play an active hands-on role in expansion of Cell2Cures current QC platform, in collaboration with Cell2Cures existing team, and external parties, and you will coordinate, plan, and perform data analysis within our existing platform.

Tasks include:

  • Implementation of new in-house QC methods based on flow cytometry, ELISA, cell culture etc.
  • Validation, qualification and maintenance of QC equipment and methods
  • Preparation and maintenance of procedures for QC analyses
  • Analysis of QC data and preparation of GMP documentation
  • Risk assessments, change control, and deviation management of QC methods
  • Design of QC analyses performed by contract laboratories


It is a precondition that you are not afraid to play an active hands-on role in implementation, troubleshooting, analysis and improvement of the associated quality system, and that you have the courage and willingness to learn.

In return, we offer you a job with multiple branches of learning, and the possibility to influence progress in collaboration with a dedicated team.


If you wish to be at the forefront of Danish translational stem cell development, where challenges are huge and the pace is fast, but commitment exceeds both, – we look forward to receiving your application.

We will process applications as we receive them and will have interviews with qualified candidates as we identify them, so please send your application as soon as possible.

For any further questions, please do not hesitate to contact Annette Ekblond telephone no. +45 21 78 28 24.

Cell2Cure is currently expanding. You will be one of several new colleagues also associated with production, quality control and regulatory affairs.



As soon as possible



We look forward to receiving your application as soon as possible.