Quality Control Analyst

2 giorni fa

Fornovo San Giovanni, Italia Bidachem A tempo pieno

**THE POSITION**:
In this exciting and challenging role, you will participate in the QC area testing of raw material, in-process samples and final vaccine samples related to the production of antigens and vaccines. In addition, you will take care of the environment affected by its actions or omissions, by managing, organizing, and supervising the areas within your competence so that the environment is preserved in all its aspects. You will work in a GMP (EudraLex - Volume 4 - Good Manufacturing Practice (GMP) guidelines) environment, and therefore will respect and enforce the standard of reference, as well as for business procedures that describe it.

**Task & Responsibilities**:
- You will be responsible to conduct GMP Analysis- In this role, you will be responsible for a designated area in the QC department, and you will ensure the correct procedures are adhered to, in terms of Quality, Environment & Safety- Besides you will raise and investigate deviations and out of specifications within the QC department- Furthermore, you will promote, develop, and strive for continuous process improvements within the QC department including method development and evolving existing processes- In addition, you will write Protocols, Reports and Procedures (SOPs)- Learning of the management system of the Quality- Learning tools and procedures applied within the site- In this role you will support laboratory on the development e validation of Analytical processes

**Requirements**:
- Previous experience in Quality Control in Chemical-Pharma Industry (minimum 10 years)- Knowledge and correct use of main devices needed in a Quality Control Department: GC (Injection and Head-space), HPLC, spectrophotometers, atomic absorption/ICP-MS- You should be able to manage data flow OOX and deviations- Good knowledge of GMP and ISO- You are already familiar with audit AIFA e FDA- Good English knowledge (writing & speaking)- Available to work in shifts

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