Job Description

Position Purpose: -Shift Lead I -The Shift Leader is responsible for managing his team to carry out the manufacturing operations according to schedule in compliance with HSE and GMP rules. -Process Specialist / Equipment Specialist -Execute assigned manufacturing tasks and activities according to production schedule to enable the timely production of product with the quality and quantity in compliance with the relevant GMP, safety and environmental guidelines. -Documentation Specialist GMP -The Documentation Specialist GMP reviews and consolidate the Batch records after production in order to deliver them to Quality Assurance acc. to set timelines & in right quality. The Documentation Specialist GMP performs entries and verifies transactions/declarations in the ERP system. Major Accountabilities: -Shift Lead I -Represent production management to the team members and promote Novartis values within the team -Line responsibility and shift walkthrough -Engage and motivate the team and delivers strong results with an empowered team -Process Specialist -Participation to the manufacturing processes -Participation to the manufacturing processes -Perform all Equipment Operator Tasks/Responsibilities -Perform all Equipment Operator Tasks/Responsibilities -Shift supervision, team coordination planning & support where shift-lead does not exist or when shift lead is absent -Perform operators on-boarding, training and training status follow-up -Equipment Specialist -Participation to the manufacturing processes -Participation to the manufacturing processes -Perform all Equipment Operator Tasks/Responsibilities -Perform all Equipment Operator Tasks/Responsibilities -Suggest improvement actions (organization, process, safety, hygiene, etc.) at shop floor -Documentation Specialist GMP -Prepare, print and consolidate the batch documents, labels... and handover to production operators within the deadlines set according to the production schedule -Follow up on updates and versions of documents in production (procedures and logbooks) -Manage the documents review and approval cycle -Complete the ERP (SAP) and RFT (right first time) databases, make available and participate in the analysis of trends and performance indicators -HSE and Quality -Promote and improve the Safety and Quality cultures -Ensure overall inspection readiness for area of responsibility -Participate in HSE risk assessments -KPI and Data Reporting for process teams -Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt -Distribution of marketing samples (where applicable) Diversity & Inclusion / EEO We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements Operations Management and Execution Collaborating across boundaries Functional Breadth English Transportation Manufacturing Process Execution General HSE Knowledge Knowledge of GMP

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