" As a candidate, I appreciated not only 3HR's professionalism but also their availability. I would not hesitate to recommend their services. "

Bilguissou D. - CQV Engineer

" From the initial phone call to my first day on the job, the follow-up has been outstanding. "

François F. - Process & CQV Engineer

" Gwendoline was able to find the perfect match for my professional career, I thank her for her listening and professionalism, I recommend 3HR. "

Kathleen G. - Communication & Internal Relations Manager

" Listening, competent, fast and gives very good advices. "

Alexandre T. - CQV Engineer

Freelance or temporary QA & RA Officer for PMO - Biotech

Liège

Contract :

Temporary

Schedule :

Full-time

Organisation size :

11-50

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. holding a Bachelor's degree in Life Science 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

If you’re looking for an opportunity to make a significant impact to the lives of patients by helping companies develop robust CRYO-processes, from raw material to the hospital bedside, then we’d love to hear from you!

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