Qc Pds Ad - Frosinone, Italia - Thermo Fisher Scientific
Descrizione
Requisition ID:
When you're part of the team at Thermo Fisher Scientific, you'll do important work, like helping customers in finding cures for cancer, protecting the environment or making sure our food is safe.
Location/Division Specific Information
Ferentino, Italy
How will you make an impact?
The QC PDS AD&GMP Technician is a hands-on role including the testing of raw material, API / DS, semi-finished and finished products (Release and Stability)
What will you do?
- Ensures the execution of analytical laboratory analyses in accordance with GMP requirements, relating to API / DS, semifinished and finished products (Release and Stability)
- Analytical laboratory techniques to be executed: physical tests (pH, KF, Osmolality), Chromatographic tests (HPLC/UPLC) and biochemical analysis (cIEF, SDS-Page, Dot-Blot, RT-PCR)
- Ensures the execution of analytical methods validation/transfer
- Reference standard, reagents and laboratory materials management
- Working to deep insights in experimental data, complex analytical studies, and other to solve existing problems within the laboratory work environment, prevent potential problems, and to help existing systems run more efficiently and effectively.
- Assist client in data sharing of complex study and testing cooperating with Scientist of the team and TL.
- Reinforce the problem solving to facilitate Scientist's projects management and TL activities coordination.
- Work on data review and technical analytical documentation
- Ensure the control of all is needed to manage testing and activities, even if responsibility of the other analysts, such as reference standard, columns presence etc.
How will you get here?
Education
Degree in CTF, Chemistry, Biology or other similar fields
Diploma Chemical/Laboratory technician certificate
Experience
- Experience in pharmaceutical industries
- 1 years of experience in Quality Control
Knowledge, Skills, Abilities
- Knowledge of the main techniques of chemicalphysical and biochemical analysis and validation of analytical methods
- Knowledge of GMP and national/international regulations
- Good problemsolving abilities
- Proficiency in Microsoft Office suite and analytical software (Empower, LIMS)
- Be prepared to work with conflicting priorities, under time constraints and in a dynamic team environment
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