**THE POSITION**:
**For this position we offer an initial one year contract with external agency.
***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
- 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

📌 Quality Control Junior Analyst (Fornovo San Giovanni)
🏢 Bidachem
📍 Fornovo San Giovanni