Pilot Plant Quality Control Associate Expert

Novartis Pharma Schweiz; Ivrea; In loco; EUR 30.000 - 40.000; Tempo pieno

Descrizione del lavoro

A leading pharmaceutical company in Ivrea is seeking a Pilot Plant Quality Control Associate Expert to execute analyses on various pharmaceutical products. Responsibilities include conducting stability studies, collaborating with QA, Production, and R&D, and ensuring GMP compliance. The ideal candidate will have a degree in Chemistry and previous laboratory experience. Proficiency in English and Italian is required for this full-time role, which offers opportunities for career advancement.

Competenze

• Degree in Chemistry is mandatory.
• Previous experience in a laboratory environment required.
• Solid technical knowledge of pharmaceutical/chemical QC is essential.

Mansioni

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

Conoscenze

GMP compliance

Data integrity

Analytical techniques

Laboratory experience

Fluent in English

Fluent in Italian

Formazione

Degree in Chemistry

Descrizione del lavoro

Pilot Plant Quality Control Associate Expert

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• 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.
• 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

Seniority level

Entry level

Employment type

Full-time

Job function

Management and Manufacturing

Industries

Pharmaceutical Manufacturing