QC Technician (m/f)

Your responsibilities

As a QC Technician, you will be in charge of operational activities related to the development and validation of analytical methods, quality control of batches of the NOVADIP-BIOSCIENCES’s novel regenerative medicines. Your main responsibilities are as follows:

  • Performing analytical method development, qualification and validation.
  • Performing quality control testing (including reporting and validation).
  • Controlling and maintaining the environment (equipment and facilities).
  • Writing, checking and validation of protocols related to QC activities.
  • Ensure compliance to GMP requirements and laboratory procedures.
  • Managing logistic tasks related to QC activities.

Your profile

  • Bachelor or Master Degree in Biotechnology/Biology or equivalent relevant experience.
  • Hands on experience in a cGMP environment is mandatory.
  • Very good theoretical knowledge and practical experience in cell culture, immunoassays (ELISA, Flow cytometry, immunohistochemistry) and bioassays are mandatory.
  • Hands on experience in stem cell culture is a strong asset.
  • Knowledge and experience in molecular biology (PCR, Q-PCR) is an asset.
  • Flexible, concerned about the quality of work and respectful of planning.
  • Good knowledge of Microsoft Word and Excel.
  • Rigorous, well-organized, meticulous and conscientious person with excellent teamwork spirit and interpersonal skills.


  • A full-time permanent position (40h/week) in a growing team.
  • To work in a human-sized, dynamic, respectful and professional environment.
  • The opportunity to take part in a challenging scientific and business growth.
  • An attractive salary package with several advantages.

Please use the button above email your CV together with an adapted cover letter to careers@novadip.com. Your application and related information will remain strictly confidential.