QC Lab Technician

JR France; Valence; À distance; EUR 40 000 - 60 000; Plein temps

Résumé du poste

Une entreprise recherche un Technicien QC en laboratoire spécialisé dans la validation des instruments et les tests d'endotoxines. Vous travaillerez à distance dans un projet à fort impact, soutenant des équipes à travers l'Europe. Une expertise en SoftMax Pro est essentielle, ainsi que d'excellentes compétences en communication. Rejoignez-nous pour faire la différence dans le domaine des sciences de la vie.

Qualifications

• Expérience en validation d'instruments de laboratoire dans des environnements GxP.
• Compétences en rédaction et gestion de documents.
• Langue anglaise requise (français ou allemand un plus).

Responsabilités

• Coordonner les mises à jour logicielles et préparer la documentation de validation.
• Concevoir et exécuter des tests d'acceptation utilisateur.
• Former et soutenir les utilisateurs sur les systèmes de validation.

Connaissances

lab instrument validation

endotoxin testing

data integrity

User Acceptance Testing (UAT)

communication skills

Outils

SoftMax Pro

Biomerieux

Lonza

Description du poste

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Remote Contract Opportunity – QC Lab Technician (Endotoxin Testing)

? Remote (France or Europe-based) | ? Start Date: June | ? English (French or German a plus)

Are you an experienced QC systems consultant with a background in lab instrument validation and endotoxin testing ? We’re seeking a skilled professional to support the deployment and maintenance of a QC Core Model used across multiple European sites.

? Your Mission

As a key part of the team, you’ll provide expert support on lab instrument software systems , focusing on SoftMax Pro and Endotoxin testing solutions (Biomerieux or Lonza). Your role will be essential in ensuring system integrity, compliance, and user readiness across multiple sites.

• Coordinate major/minor software upgrades (SoftMax Pro & endotoxin testing platforms)
• Draft/update User Requirements Specifications (URS) with a focus on data integrity
• Prepare and maintain validation documentation:
• Validation plans, test strategies, risk assessments, traceability matrices
• Lead User Acceptance Testing (UAT) : design, scripting, execution, and reporting
• Support sites in defining local validation requirements
• Prepare training materials and ensure SOPs/instructions are in place
• Liaise with cross-functional teams to gather feedback and guide system deployment
• Strong experience in lab instrument software validation within GxP environments
• Familiar with endotoxin testing systems and microplate reader tools
• Proven track record in documentation, UAT coordination, and user training
• Excellent communication skills in English (French or German is a strong advantage)
• Available to start in June and work remotely within France or Europe

Interested in joining a high-impact project with a global reach?

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