Quality Control Analyst.

For our client, we are looking for a QC Analyst (FR) to join their team in Neuchâtel.

Work Conditions:

• On-site role in Neuchâtel
• 6-month contract via Randstad (17/03/2025 - 16/09/2025)
• French mandatory (English is a plus)
• Variable working hours, including weekends (1 out of 4 to 6) and on-call periods

Job Responsibilities

As the entry point for the Quality Control (QC) laboratories, you will be responsible for providing the necessary samples, stability materials, and articles for analysis. You will ensure the proper handling, documentation, and distribution of samples while maintaining compliance with Good Manufacturing Practices (GMP) and internal procedures.

Your main tasks will include:

Sample Handling & Logistics

• Control, aliquot, identify, record, distribute, store, or dispose of samples in compliance with GMP and standard operating procedures (SOPs)
• Ensure proper reception, processing, and distribution of samples according to established guidelines
• Receive and register samples in tracking systems (LIMS or similar) within defined timelines
• Perform sample destruction and transfers as required

Stability & Validation Studies

• Participate in validation protocols and stability studies, from sample reception to analysis, stabilization, and disposal
• Ensure proper documentation and traceability of stability samples

Stock & Equipment Management

• Manage the stock of consumables and reagents for the laboratory
• Oversee equipment maintenance, calibration, and temperature alarm monitoring
• Ensure proper logbook completion and review

Regulatory Compliance & EHS

• Adhere to GMP guidelines and internal quality procedures
• Support regulatory audits by maintaining accurate documentation
• Follow EHS (Environment, Health & Safety) regulations and actively report any deviations

Support for QC Teams

• Assist with non-testing tasks such as preparation of analysis solutions, freezer transfers, and autoclaving activities
• Collaborate with cross-functional teams for efficient sample processing

Job Requirements

? Education & Experience

• Previous experience in sample management, stability studies, or QC logistics within a GMP-regulated environment
• Familiarity with Good Manufacturing Practices (GMP), stability management, and laboratory sample handling
• Experience with LIMS or other sample tracking systems is a plus

? Technical & Soft Skills

• Strong attention to detail and ability to follow SOPs precisely
• Excellent organizational and multitasking skills
• Proactive mindset in ensuring regulatory compliance and safety standards
• Ability to work both independently and in collaboration with QC and regulatory teams

This is a great opportunity to join a dynamic and high-quality environment. If you meet the requirements and are interested, apply now!