Location: 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 Role Role Responsibilities: Operational Ensure all activities in compliance with cGxP, incl.
data integrity Review and approval of analytical data / tests (analytical release) Maintain and calibrate equipment incl.
plan preparation Support sample planning and sampling execution Stability testing (projects) – protocol preparation, evaluation, report preparation Performance of stability studies, protocols and comparative reports for supplier qualification HSE Comply with all HSE guidelines Detect and report potential accident, risks and propose solutions Participate in HSE risk assessments Preparation and participation to internal HSE audits Responsible for participating in initial training and retraining Ideal Background: 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 experience Languages: Good (oral and written) in English; fluent in local language (oral and written) Commitment 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.
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