REQ-10068760
дек 16, 2025
Италия

Сводка

Location: Ivrea, Italy #onsite

Role Purpose:
This role utilizes chemistry laboratory skills to test and measure product or materials while ensuring that analysis is performed according to established Standard Operating Procedures (SOPs), Analytical Methods & current Compendia.

About the Role


Key responsibilities:

  • Executes analyses on excipients, raw materials, finished products, and packaging per internal SOPs and applicable pharmacopeias.
  • Conducts stability studies, process and method validations, and activities related to tech transfer of pharmaceutical products.
  • Performs instrument qualification and re-qualification (IQ/OQ/PQ) according to internal procedures.
  • Records analytical data in compliance with ALCOA+ principles and data integrity requirements.
  • Reviews GMP documentation, batch records, analytical reports, and certificates for completeness and compliance.
  • Collaborates with QA, Production, and R&D; supports method transfers, troubleshooting, and safe lab/5S practices.
  • Participates in audits and inspections by providing data and responses; contributes to CAPA, deviations, change control, and SOP updates.
  • Tracks KPIs: on-time completion and right-first-time rates, data integrity compliance, audit outcomes, documentation quality, and continuous improvement impact.

Essential Requirements:

  • Degree in Chemistry
  • Solid technical-scientific knowledge of pharmaceutical/chemical QC or equivalent analysis
  • Previous experience working in a laboratory environment in the pharmaceutical industry
  • Experience in GMP environment
  • Fluent in Italian and English

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? https://www.novartis.com/about/strategy/people-and-culture

Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards

Development
Development
Италия
Ivrea
Research & Development
Full time
Regolare
No
Two business people with a laptop.
REQ-10068760

Pilot Plant Quality Control Associate Expert

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