Pilot Plant Quality Control Associate Expert

Novartis Contract Manufacturing; Ivrea; In loco; EUR 30.000 - 40.000; Tempo pieno

Descrizione del lavoro

A leading pharmaceutical company is seeking an entry-level laboratory technician in Ivrea, Piemonte. The role involves executing analyses on pharmaceutical products, conducting stability studies, and ensuring compliance with GMP standards. Candidates should hold a degree in Chemistry and be fluent in Italian and English. This full-time role offers a chance to contribute to advancing medical solutions.

Servizi

Diversity and Inclusion commitment

Comprehensive benefits and rewards

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.
• Tracks KPIs: on-time completion and right-first-time rates, data integrity compliance.

Conoscenze

Chemistry laboratory skills

Technical-scientific knowledge of pharmaceutical QC

Experience in GMP environment

Fluent in Italian

Fluent in English

Formazione

Degree in Chemistry

Descrizione del lavoro

Overview

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

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?

Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture

You will receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits-rewards

Commitment to Diversity and Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams representation of the patients and communities we serve.

Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network

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. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture

Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network

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

Seniority level

• Entry level

Employment type

• Full-time

Job function

• Management and Manufacturing
• Industries: Pharmaceutical Manufacturing

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