• support in the implementation of protocols reports and documents and ensure their management according to current GMP, SOPs and guidelines.
• perform analyses following specified instructions from team leader and supervisor, SOPs and analytical procedures
• perform cleaning method validation and sampling in production area
• perform other duties and support activities as assigned
• be compliant with all job related safety and other training requirements
• provide testing support for production of sterile injectable drugs
• learn to perform analysis effectively and in GMP compliance, mainly with chromatography and spectrophotometry
• manage and dispose samples
• preparing chemical solutions

Skills and Abilities

• Ability to work independently and as a member of a cross-functional team
• Willingness to learn, be mentored and improve
• Desire to understand and improve current practices
• Focus on timelines and on time completion
• Self-motivated and detail oriented
• Must be able to work safely with chemicals, biologics and hazardous materials

Qualifications

• Previous experience in lab setting is strongly preferred
• Ability to perform common chemical analysis, experience in chromatography and spectrophotometry is strongly preferred
• English and italian languages (professional knowledge)
• Knowledge of the main chemical techniques (HPLC, GC, UV...)
• Excellent knowledge of Office Suite