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Offerte di Lavoro Novartis in Piemonte

1 - 15 di 15
1 - 15 di 15
Risultati di Ricerca - Lavoro Novartis in Piemonte
Novartis Farmacéutica-Ivrea
Novartis Farmacéutica is seeking a QA Officer in Ivrea, Italy, responsible for quality oversight in GMP activities. You will work shifts, including nights and weekends, ensuring compliance with quality standards. This role requires a scientific...
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Manpower-Ivrea
una corretta allocazione degli ordini nel rispetto dei requisiti normativi e qualitativi. Principali responsabilità  •  Gestione e analisi dei dati secondo i processi e le linee guida Novartis, sia locali che globali...
Novartis Farmacéutica-Ivrea
Available to work in shifts, including night shifts and weekends.  •  Fluent in Italian.  •  Good knowledge of English. Commitment to Diversity and Inclusion Novartis is committed to building an outstanding, inclusive work environment and diverse teams...
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Novartis Farmacéutica-Ivrea
and procedures. Support qualification and validation activities by managing and reviewing the related documentation. Ensure the compliance of all business areas with the Novartis Quality Manual and Policies and all relevant GxP, legal and regulatory requirements...
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Novartis Farmacéutica-Ivrea
Novartis Quality Manual.  •  Ensure effective tracking, escalation, and timely closure of CAPAs, including proactive management of risks related to delayed or ineffective actions.  •  Prepare, review, approve, and manage GxP documentation lifecycle activities...
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Novartis Farmacéutica-Ivrea
Novartis Farmacéutica in Ivrea, Italy is seeking a Quality Assurance professional to ensure compliance in sterile pharmaceutical manufacturing. You will oversee manufacturing lines validation activities and coordinate the QA team during operations...
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Novartis Farmacéutica-Ivrea
in major markets of assigned products.  •  Report technical complaints, adverse events, or special case scenarios related to Novartis products within 24 hours of receipt. Minimum Requirements  •  BSc. in Chemical Engineering, Pharmaceutical Technology, or an...
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Novartis Farmacéutica-Ivrea
and leveraging of best practices and expertise within the Novartis engineering community.  •  Lead the implementation of technology strategy and the approved equipment and project execution standards. Leadership & Organization  •  Be available, accountable...
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Novartis Farmacéutica-Ivrea
Novartis Farmacéutica in Ivrea, Italy is seeking a qualified professional to support the pilot plant ramp up and operationalization process. Responsibilities include ensuring compliance with quality systems, managing documentation, and supporting...
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Novartis Farmacéutica-Ivrea
Novartis Farmacéutica in Ivrea is seeking an Engineering Lead responsible for managing engineering processes and investment projects. The candidate will ensure compliance with regulatory standards and improve the reliability of production plants...
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Novartis Farmacéutica-Ivrea
Novartis Farmacéutica is seeking a Qualified Person in Ivrea to supervise manufacturing processes and ensure compliance with local regulations. This role guarantees that each batch of medicines produced meets all legal and quality standards. The...
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Novartis Farmacéutica-Ivrea
Novartis Farmacéutica is seeking an Isotope Project Lead in Ivrea, Italy. The role involves managing projects related to radioisotope production and purification, collaborating closely with development centers and Contract Manufacturing...
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Novartis Farmacéutica-Ivrea
Novartis Farmacéutica in Ivrea, Piemonte, is seeking a QC Supervisor to support the QC Head in managing quality control operations. Responsibilities include overseeing analytical activities, ensuring compliance with regulations, and managing QC...
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Novartis Farmacéutica-Ivrea
The QC Supervisor supports the QC Head to ensure that Quality Control processes for materials acceptance, batches, quality control and QC equipment validation/qualification are executed and fully compliant to cGMPs regulation, corporate and national...
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Novartis Farmacéutica-Ivrea
Independently supervise, without third‑party interference, manufacturing processes and control testing related to the drug manufacturing license, operating as Qualified Person in accordance with Article 52 of Legislative Decree n. 219 of 24 April...
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