Pilot Plant Quality Control Associate Expert

Novartis ACC; Ivrea; In loco; EUR 40.000 - 60.000; Tempo pieno

Descrizione del lavoro

A global pharmaceutical company in Ivrea is seeking a Chemistry Laboratory professional. The role includes executing analyses on excipients, raw materials, and finished products while adhering to internal SOPs. Candidates must possess a Chemistry degree, solid knowledge of pharmaceutical quality control, and experience in a GMP environment. Fluency in Italian and English is required. Join us in making a difference in patients' lives!

Servizi

Competitive salary

Comprehensive benefits package

Professional development opportunities

Competenze

• 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.

Mansioni

• Executes analyses on excipients, raw materials, finished products, and packaging per internal SOPs.
• Conducts stability studies, process and method validations, and activities related to tech transfer of pharmaceutical products.
• Performs instrument qualification and re-qualification according to internal procedures.
• Records analytical data in compliance with ALCOA+ principles and data integrity requirements.
• Reviews GMP documentation and analytical reports for completeness.
• Collaborates with QA, Production, and R&D; supports method transfers and troubleshooting.
• Participates in audits and inspections by providing data.
• Tracks KPIs such as on-time completion and documentation quality.

Conoscenze

Laboratory skills

Analytical skills

Fluency in Italian

Fluency in English

Knowledge of pharmaceutical/chemical QC

Formazione

Degree in Chemistry

Descrizione del lavoro

Summary

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