CSV
- France
- Contract
- CAPEX Projects
This vacancy has now expired
Profil recherché:
- 5 à 10 ans d'expérience en validation de systèmes informatisés lié aux équipements de laboratoire
- Expériences en écriture d'URS, de risk assessment, protocolo IOQ
- Expérience avec les équipements suivants : Mass Spectrophotomètre, Cellometer, electrophoresis, Infrared SPectrophotometer, colony counter, PCR, Protein simple analyser, enceintes thermostatées
Rôle:
Vous intégrerez l'équipe de génération des documents de qualification/validation des systèmes informatisé liés aux équipements de laboratoires sur le site de notre client situé à Toulouse.
- Ecrire des documents liés à la validation des systèmes informatisés d'équipement de laboratoire (URS, Data Intégrité Assessment, Risque Assessment, Protocol IOQ)
- Support de gestion des non-conformités de qualification (investigation, assessment, proposition de CAPA)
- à la demande: Exécution les protocoles de qualification en support de l'équipe/Support de l'équipe CQV pour réaliser les tests de qualification en lien avec la CSV.
#LI-CO1
Once again can I via you recognise the superb support I was given before, during and after this short contract. The support, was as usual professional and every friendly.
QA Specialist
We have worked together with QCS Staffing for seven years now and have always received a professional service. QCS Staffing's speciality certainly lies within their technical sourcing abilities and they have met our demanding requirements time and time again. Coupled with this are the integrity of QCS Staffing's people and their ability to deliver.
Global Pharmaceutical firm
I have always received a highly professional & personable service from the team at QCS Staffing. They listen carefully to the specific requirements of available roles and work tirelessly to supply a pool of potential candidates and make the hiring and contract renewal process an easy activity to manage.
Global Pharmaceutical firm
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Caroline
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