Qc Senior Scientist

SummaryLocation: Ivrea, Italy

Role Purpose:
Specialist in the area of analytics, supporting the laboratory team with in-depth knowledge to ensure efficient performance of laboratory activities and related investigations in compliance with GxP and HSE guidelines. Performs review and approval of analytical data.

About the RoleRole Responsibilities: Operational OOx/deviation handlingCAPA definition/KPI trendingEnsure all activities in compliance with cGxP, incl. data integrityReview and approval of analytical data / tests (analytical release)Maintain and calibrate equipment incl. plan preparationSupport sample planning and sampling executionStability testing (projects) – protocol preparation, evaluation, report preparationPerformance of stability studies, protocols and comparative reports for supplier qualificationReview and approval of analytical tests (analytical release)HSE Comply with all HSE guidelinesDetect and report potential accidents, risks and propose solutionsParticipate in HSE risk assessmentsPreparation and participation in internal HSE auditsResponsible for participating in initial training and retrainingIdeal Background: Relevant Experience
Professional experience (3-5 years) in the pharmaceutical sector or in the manufacture of active substances in analytical laboratories in a GMP environment or equivalent; Collaborating across boundaries; Functional Breadth; efficient inter and intra-departmental communications.Education & Qualification
Technical education & 3-5 years relevant experience or Desirable University degree in Pharmacy or Chemistry or equivalent + 0-4 years working experienceLanguages
Good (oral and written) in English; fluent in local language (oral and written)Breakthrough Analysis; Being Resilient; Operational Excellence; Continuous Learning; Digital & Tech SavvyMS Office applications and other standard IT applications supporting Quality activitiesLaboratory equipment; Quality Control (QC) Testing; Quality Control Sampling; Knowledge of TQM and related industry GxP standards and processes; Laboratory Excellence; Quality decision makingCommitment to Diversity and Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients' lives. Ready to create a brighter future together?
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Division: International
Business Unit: Innovative Medicines
Location: Italy
Site: Ivrea
Company / Legal Entity: IT58 (FCRS = IT058) AAA Italy Srl.
Functional Area: Research & Development
Job Type: Full time
Employment Type: Regular
Shift Work: No
Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

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