QC Validation Expert

  • Location: Charleroi
  • Type: Perm
  • Job #14860

QC Validation Expert

Charleroi – contracting

What are your responsibilities?

The QC Validation Expert  main role is to implement and maintain the QC infrastructure & equipment in the Quality Control department. He reports to the QC supervisor infra & equipment. In order to fulfill his role, he:

  • Is involved in the QC equipment management in partnership with technical service and quality control operations (order, installation, maintenance, qualification..)
  • Drafts/reviews QC documents linked to equipment qualification (URS, IQ/OQ/PQ, instructions, Change control,…)
  • Acts as an interface with subcontractors in partnership with technical service
  • Is involved in the installation, modifications and improvements of QC lab infrastructures
  • Is involved in EMS management  
  • Takes the lead on deviations/CAPA regarding QC equipment, EMS and infrastructure
  • Takes part to internal and/or external audits, if necessary
  • Maintains an open and effective communication with all other QC team members and with other departments (Production, QA, and Technical Service)
  • Functionally manages QC supports

Who are you?

  • Graduate level in chemistry, biochemistry, clinical chemistry, biology, etc.
  • At least 2 year’s experiences in cGMP environment
  • At least B1 English level
  • Organization skills, multitasking
  • Quality minded, autonomous, rigorous, attentive to details, persevering and pro-active
  • Teamwork and teaching skills
  • Good communication skills 
  • Computer skills: Microsoft Office, Ms Teams

What can you expect?

Jefferson Wells offers you a permanent contract within a growing and dynamic biotech company. You will work in a human-sized working environment with convivial atmospheres and scientific challenges. You’re interested in this job? We kindly invite you to apply or send your CV, [email protected]

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