Job description Our client a pharmaceutical company in Basel is looking for an QC Analyst Start Date: ASAP

Location:

Basel Duration: 1 year with possibility of extension Workload:
Workload: 80% - 100% Your

Responsibilities:

Sample storage and management Analytical testing and documentation of API / drug substance and raw materials (e.g. HPLC, Titration, pH, Osmolality, TOC/TN) Ensure all activities in compliance with cGxP, incl. data integrity Stability (when not centralized) Testing/Sample storage and management Analytical documentation of stability samples to cGxP standards Comply with all HSE guidelines Detect and report potential accident, risks and propose solutions Kesponsible for participating in initial training and retraining

Your profile:

Previous experience working in a laboratory environment in the pharmaceutical industry (quality assurance, production), aseptic technique. Completed apprenticeship as a laboratory assistant or equivalent training Languages Basic (oral... and written) in English; fluent in local language (oral and written) Collaboration; result-oriented Administrative activities and GMP and HSE-compliant, efficient production and documentation of standardized tasks in the infrastructure Breakthrough Analysis;
Being Resilient;
Operational Excellence;
Continuous Learning;
Digital & Tech Savvy Laboratory equipment;
Quality Control (QC) Testing;
Quality Control Sampling; knowledge of TQM and related industry GxP standards and processes;
Laboratory Excellence;
Quality decision making
Basel Switzerland

Salary Criteria