Pilot Plant Quality Control Associate Expert

Novartis; Ivrea; In loco; EUR 30.000 - 45.000; Tempo pieno

Descrizione del lavoro

A leading pharmaceutical company is seeking a Quality Control Analyst in Ivrea, Italy. The role involves utilizing chemistry laboratory skills for testing and analysis according to established procedures. Ideal candidates should hold a degree in Chemistry and have experience in a GMP environment. Fluency in Italian and English is essential. This full-time position offers the opportunity to collaborate with various departments and contribute to continuous improvement efforts.

Competenze

• Fluent in Italian and English.
• Solid technical-scientific knowledge of pharmaceutical/chemical QC.
• Previous experience in a laboratory environment.

Mansioni

• Executes analyses on excipients, raw materials, and finished products.
• Conducts stability studies and method validations.
• Collaborates with QA, Production, and R&D.

Conoscenze

Laboratory skills

Analytical methods

Data integrity

GMP compliance

Collaboration

Formazione

Degree in Chemistry

Descrizione del lavoro

Job Description Summary

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.

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 a GMP environment.
• Fluent in Italian and English.

Employment Type: Full‑Time

Experience: years

Vacancy: 1