An. Support
The candidate will be part of a dynamic and result-driven environment and will have the possibility to gain and in-depth experience of a GMP Quality control lab focused on new projects and technology tranfers. 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 proceduresperform other duties and support activities as assignedbe compliant with all job related safety and other training requirements. provide testing support for production of sterile injectable drugslearn to perform analysis effectively and in GMP compliance, mainly withchromatography and spectrophotometrymanage and dispose samplespreparing chemical solutionsSkills and AbilitiesAbility to work independently and as a member of a cross-functional teamWillingness to learn, be mentored and improveDesire to understand and improve current practicesFocus on timelines and on time completionSelf-motivated and detail orientedMust be able to work safely with chemicals, biologics and hazardous materialsQualificationsMsc in Chemistry or Chemical and Pharmaceutical Technologies (or similar fields)Previous experience in lab setting is strongly preferredAbility to perform common chemical analysis, experience in chromatography and spectrophotometry is strongly preferredEnglish and italian languages (professional knowledge)Knowledge of the mail chemical techniques (HPLC, GC, UV. . . )Excellent knowledge of Office Suite
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