Summary
Execution of assigned tasks in the quality control laboratory in accordance with cGxP regulations. Performance of laboratory specific activities such as analyses, maintenance, calibration and qualification of analytical equipment.
About the Role
OPERATIONAL
- Sample storage and management
- Analytical testing and documentation of incoming materials / drug products / stability / packaging material samples
- Ensure all activities in compliance with cGxP, incl. data integrity
- Stability
- Testing/Sample storage and management
- Analytical documentation of stability samples to cGxP standards
HSE
- Comply with all HSE guidelines
- Detect and report potential accident, risks and propose solutions
- Responsible for participating in initial training and retraining
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Division
International
Business Unit
Innovative Medicines
Location
Italy
Site
Ivrea
Company / Legal Entity
IT58 (FCRS = IT058) AAA Italy Srl.
Functional Area
Quality
Job Type
Full time
Employment Type
Regular
Shift Work
No