LIMS Quality Control Analyst

LIMS Quality Control Analyst

We\’re seeking an experienced QC Analyst (m/f/d) to join the newly established \“QC Digital Backbone – Master Data Management\“ team. In this vital role, you\’ll support the creation, maintenance, and governance of master data within Quality Control systems—particularly LabWare LIMS—ensuring compliance with GxP standards.

This is an excellent opportunity for someone with a strong Quality Control and LIMS background who wants to make a real impact in digital data processes within the pharmaceutical/biotech sector.

Start Date: ASAP
Location: Kaiseraugst (2 days home office per week)
Duration: 2 years (extension highly likely)
Workload: 100%
Department: QC Digital Backbone – Master Data Management (MMQIAB8R)
Environment: GMP-regulated, 9-person team

Must Haves

• Completed education (technical degree, BSc or MSc) in biotechnology, chemistry, or a related field
• Minimum 3 years of experience in Quality Control
• Minimum 3 years of experience in a GMP-regulated environment
• Strong hands-on experience with LIMS systems (ideally LabWare)
• Confident working with common IT systems in pharma environments
• Fluent in German; English a plus
• A team player with excellent communication skills and a strong sense of quality and accountability
• Structured, self-driven, and detail-oriented mindset

Responsibilities

• Create and maintain local and, where necessary, global master data within responsible systems (Single LIMS, Aspire & Speca) in compliance with GxP rules
• Ensure timely, accurate, and compliant execution of QC data management activities
• Provide system support including incident management, documentation, and reporting
• Act as a consultant for system and process-related expertise
• Participate in audits and self-inspections
• Collaborate closely with cross-functional QC and IT teams to drive digital excellence