Quality Control Analyst 865

ProductLife Group is growing and we are looking for the next member of the Medical Device international team :

About us

Group 10
Responsibilities

The main activities of this position will be:

  • Perform daily laboratory activities related to release and stability testing
  • Analyse results
  • Verify data (double check)
  • Work with other analysts in organizing the release and stability analyses of the laboratory
  • Follow up deviations, incidents and validate the results within a LIMS system.

All these activities will be performed in compliance with the GMP/HSE rules and with the regulatory requirements for each development phase of the product.

Group 11
Education

  • Bachelor degree (or master’s degree), in biochemistry or in analytical chemistry

Group 12
Experience

  • At least 5 years of equivalent experience in the biotech industry
  • A good experience and expertise in at least the following analytical techniques: chromatography (HPLC/UPLC) applied to proteins and capillary electrophoresis (CGE, iCE).

Group 13
Skills

  • Laboratory skills or quality skills
  • A good knowledge of GMP standards in QC laboratory
  • Good interpersonal, verbal, and written communication skills with ability to balance multiple priorities
  • Good knowledge of English (ability to read scientific documents)
  • Well organized, flexible, meticulous and rigorous, proactive, with a strong team spirit
  • Able to work in a multicultural environment.

Quality Control Analyst 865