Freelance or temporary QA & RA Officer for PMO - Biotech

The company

Based in the Center of Liège, our client, a spin-off of the ULg, has developed unique combination of services in CRYO-biology, cell therapy production and biologistic to support biotech companies.

With a team of 20 people, their innovative technology is based on cryopreservation in EU and US offering an integrated set of GMP services in line with the regulatory, quality and GMP requirements of the cell therapy industry.

Do you want to work in a spin-off offering a growing and multidisciplinary work environment within an international team of experts ?

 

Your role

In team, develop, deploy and monitoring the company’s policy and quality standards according to international regulations (GMP, GTP, GDP) and standards (ISO, ICH):

  • Contribute to create the Global Quality Management System and deploy it in local entities
  • Develop the related global trainings
  • Providing QA oversight over the product/process life cycle
  • Provide regulatory advice and guidance to the teams
  • Provide support to local operations QA team
  • Provide quality engineering support to internal projects (innovation and technical transfer teams)

We offer clear and concrete guidance to grow within the role, opportunities to work at HQ and/or local level, in Belgium and/or abroad in an international entrepreneur environment, where you can have impact.

You are

  • experienced in QA & RA activities in Life sciences, especially cell therapy
  • bilingual French & English
  • Min. Bachelor in Life sciences or related
  • available from now (or ASAP) until end of August 2022
  • Freelance or looking for a temporary contract

Your application

If you’re interested in joining this team, please send to Mrs Gwendoline de Robiano:

  • your resume
  • cover letter,
  • both in English

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