QC Lab Technician

JR France; Annecy; À distance; EUR 40 000 - 65 000; Plein temps

Résumé du poste

A leading life sciences consulting firm is seeking a skilled QC Lab Technician to provide expert support on lab instrument software systems focusing on endotoxin testing solutions. This remote opportunity allows you to contribute to high-impact projects across multiple European sites, ensuring system integrity and compliance. Ideal candidates will possess strong experience in GxP environments and excellent English communication skills.

Qualifications

• Experience in lab instrument software validation within GxP environments.
• Proven track record in user acceptance testing and documentation.
• Excellent communication skills in English; French or German is a strong advantage.

Responsabilités

• Coordinate software upgrades and draft User Requirements Specifications.
• Prepare and maintain validation documentation and lead User Acceptance Testing.
• Liaise with cross-functional teams to guide system deployment.

Connaissances

Lab instrument validation

Endotoxin testing

Communication in English

Documentation

UAT coordination

Outils

SoftMax Pro

Lab instrument software

Microplate reader

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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