PRODUCT STEWARD
Descrizione dell'offerta di lavoro
Ensures seamless flow of knowledge and information across functions and with other Sites when applicable with focus on the assigned product(s).
Provides second line technical/scientific process support.
Job Description Major Accountabilities.
Maintain the oversight and knowledge for entire manufacturing process performed on site and throughout the entire commercial lifecycle since transfer from development to date act as SPOC.
Create and maintain a product specific Quality Risk Analysis (QRAs).
Monitor all critical variables and key variables as appropriate using statistical analysis and conducting regular product specific data trending.
Ensure inspection readiness for all process related aspects of assigned products.
Track and evaluate product performance trending detect issues implementation of CAPAs Lead / support root cause investigation of process failures initiate and lead product improvement projects involving cross-functional teams.
Responsible for ensuring the continued state of validation (process cleaning ongoing verification etc.).
Provide the necessary data for the technical activities involved in transferring out a product focusing on existing knowledge through the appropriate documentation and supporting at the receiving site as needed.
Design and manage optimization projects.
Essential requirements.
Degree in Pharmacy Pharmaceutical Technology Chemistry Chemical Engineering or equivalent scientific degree.
Solid experience in process support Process Expert role on the shop floor of pharmaceutical manufacturing and/or QA/QC/MS&T.
Experience of data handling and applied statistics.
Fluent in English and Italian.
Skills Desired Assembly Language Change Control Chemical Engineering Chemistry Continual Improvement Process Cost Reduction Data Analytics Electronic Components General Hse Knowledge Including Gdp Knowledge Of Capa Knowledge Of Gmp Lean Manufacturing Manufacturing Process Manufacturing Production Pharmaceutics Process and Cleaning Validation Process Control Process Engineering Risk Management Root Cause Analysis (RCA) Scheduler Six Sigma Sop (Standard Operating Procedure)
Dettagli dell'offerta
- Novartis
- Tutta l'Italia
- Imprecisato - Imprecisato
- Imprecisato
- 02/08/2025
- 06/01/2026
Al mese disponibilità: dal lunedì al venerdì orario flessibile weekend retribuzione supplementare: bonus esperienza: steward: 1 anno (preferenziale) lingua: italiano (obbligatorio) inglese (preferenziale) disponibilità a viaggiare requisiti di lavoro requisiti: patente b, possibilmente......
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