QC Analyst (m/f/d)

Ihre Aufgaben:
• Sample storage and management

• Analytical testing and documentation of API / drug substance / drug product / finished product / Complaints / stability / packaging material samples

• 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

• Perform and document lab analysis (standard and more complex techniques)

• Support analytical investigations and OOx

• Implementation of innovative DP/DS methods from development

• Participation in co-validation activities or analytical transfers

Ihre Qualifikationen:
• Bachelor (or Master) in Biology or molecular Biology (no PHD needed)

• Experience in GMP
• Comitted to work in 6/4 shift model

Ihre Vorteile:
• A very renowned company

Projektdauer: 12 MM


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