About this role
Role Overview
- Microbiological analyses of release and/or stability of packaging materials, raw materials, semi-finished and finished products;
- Microbiological analyses of environmental monitoring of the plant (water, air, surfaces, etc.);
- Planned technological controls on the finished product in order to allow its release on the market by QPs;
- Supporting the manager in the planning of analytical activities with the aim of optimising analysis times and laboratory efficiency;
- Relevant analyses in compliance with GMP and company SOPs and analytical methods;
- Recording of analytical results in company computer systems and correct filling in of related departmental forms;
- Identification of technical/analytical problems, collaborating with your manager in their resolution;
- Verifying product quality standards by critically evaluating analytical data and identifying out-of-specification, out-of-trend or deviations from standard procedural flows, reporting them promptly to the direct supervisor;
- Maintenance of analytical instrumentation;
- Supporting the Micro Lab Manager in drafting and managing laboratory documentation and in all team-related activities.
Requirements
- Bachelor's degree preferably in science subject (biology, CTF, pharmacy, engineering)
- Ideal experience of at least 3 years as a laboratory analyst/laboratory technician in quality control in pharmaceutical manufacturing companies
- Instrumental Microbiological techniques.
Benefits
- Equal employment opportunities are offered without distinction with regard to religion, gender, sexual orientation, age, origin, disability or other relevant categories.