Quality Control Analyst

THE POSITION

In this exciting and challenging role, the candidate will participate in the QC area, supporting the management of documentation and the validation of new equipment. The candidate will be involved in defining and selecting appropriate analyses for specific raw materials and will test primary and secondary packaging materials, while also supporting the execution of analyses across different laboratory areas. In addition, the candidate will be responsible for managing, organizing, and supervising the areas within their competence to ensure that the environment is preserved in all its aspects. The role is performed in a GMP environment in compliance with EudraLex Volume 4 – Good Manufacturing Practice guidelines, requiring strict adherence to applicable standards and internal business procedures.

Tasks & Responsibilities

• Responsible for documentation required for the purchase of new equipment.
• Provide support on validation of QC equipment and relative documentation.
• Take part in defining and choosing the most suitable analyses to be performed on specific raw materials.
• Perform controls on Primary and Secondary Packaging Materials.
• Assist in performing analyses across multiple areas of the laboratory.
• Responsible for a designated area in the QC department, and ensure the correct procedures are adhered to.
• Raise and investigate deviations and out of specifications within the QC department.
• Promote, develop, and strive for continuous process improvements within the QC department including method development and evolving existing processes.
• Write Protocols, Reports and Procedures (SOPs).
• Learn of the management system of the Quality.
• Learn tools and procedures applied within the site.

Requirements

• Educational background in Chemistry Biology or similar.
• Knowledge of European Pharmacopeia and Good Manufacturing practice (GMP).
• Excellent command of the Italian and English language.
• Good organizational skills and ability to work in team/ individually.
• Ability to work methodically and carefully according to tight deadlines.
• Good IT skills especially with knowledge with Excel and Office.
• Ability to write Protocols and Reports.
• Ability to write Procedures (SOPs).

What we offer 

• For this position we offer a temporary contract of 12 months with an external agency.
• Free access to the company canteen.
• A range of benefits for physical, financial, social and mental wellbeing.
• A support to develop professional and personal paths including our full range of development programs. 

We warmly welcome applications from candidates belonging to protected categories, in accordance with Law 68/99.

We foster a workplace built on respect, trust, and empathy - free from discrimination. We are powered by our people, and we believe that our differences are our strengths. Everyone is valued, respected and empowered to be themselves.