QC Analyst (m/f/d)
We’re seeking an experienced QC Analyst (m/f/d) to join our client's 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)
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
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