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 staff.The ideal candidate holds
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 ideal candidate will
IT58 (FCRS = IT058) Advanced Accelerator Applications Italy Srl is seeking a qualified professional to manage Quality aspects and projects in Ivrea, Italy. The role involves ensuring GxP conformity and compliance within the Novartis Quality Management
Experteer Italy is looking for a Qualified Person who will oversee manufacturing processes and batch release to ensure compliance with regulatory requirements and our GMP quality system. You will play a key role in collaborating with Quality Control
Novartis Italia, located in Ivrea, is seeking a QA Officer responsible for quality oversight in GMP activities. This role involves validating production sites, responsible for batch shipment releases, and maintaining quality documentation.The ideal candidate holds a scientific degree
Calling all innovators – find your future at Fiserv. We’re Fiserv, a global leader in Fintech and payments, and we move money and information in a way that moves the world. We connect financial institutions, corporations,
Company Description Gnosis by Lesaffre aims to raise the standard of human health and build a world where proactive health solutions empower people to live longer, happier lives. By exploring the world of microorganisms, we tap
The chance to build a better future is right in front of you Do Work That Matters – Il tuo ruolo e le tue responsabilità Vuoi fare un lavoro che sia davvero significativo e di impatto?
Job Description SummaryThe QA Officer guarantees the quality oversight over the entire working time of the facility for all the ongoing GMP activities. Job Description In this role you will be required to work in shifts,
Job Description SummaryThe 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
THE INTERNSHIP For our site in Fornovo San Giovanni we are looking for a new person to join the Product Quality Assurance Department. During this formative period, you will have the opportunity to understand the role
We are the leading Tech Company in Europe, supporting digital innovation for over 45 years. We are committed to bringing digital technology into every business. How? By putting customers first and becoming the go-to partner
Job Description SummaryManage Quality aspects and projects within area of responsibility. -Ensures and supports overall GxP conformity and Compliance with the Novartis Quality Management Systems. Job Description In this role you will be required to work
THE INTERNSHIP For our site in Fornovo San Giovanni we are looking for a candidate to join Production Department, within the Production Compliance Team. During this formative period, you will have the opportunity to understand the
Growing What Matters Starts With You Corteva Agriscience serves to enrich the lives of those who produce and those who consume, ensuring progress for generations to come. We foster an inclusive culture where we encourage each
Ecco cosa farai Nel dipartimento Quality Operations del sito di Parma, contribuirai in modo decisivo allassicurazione della conformità e qualità dei nostri prodotti farmaceutici. Ti occuperai di garantire che tutti i prodotti rispettino rigorosamente le procedure
Informazioni sul ruolo Tipo di lavoro: Dipendente. Contratto: Tempo indeterminato. Località: Parma, IT. Ecco cosa farai Nel dipartimento Quality Operations del sito di Parma, contribuirai in modo decisivo allassicurazione della conformità e qualità dei nostri prodotti
Informazioni sul ruoloTipo di lavoro: Dipendente. Contratto: Tempo indeterminato. Località: Parma, IT.Ecco cosa faraiNel dipartimento Quality Operations del sito di Parma, contribuirai in modo decisivo allassicurazione della conformità e qualità dei nostri prodotti farmaceutici. Ti occuperai
Chiesi è un gruppo biofarmaceutico internazionale focalizzato sulla ricerca, con 90 anni di esperienza e presente in oltre 30 Paesi, con sede centrale a Parma, Italia. Più di 8.000 collaboratori in tutto il gruppo sono uniti
Experteer OverviewIn questo ruolo contribuirai a garantire conformità e qualità dei farmaci presso il sito di Parma, lavorando in un team multidisciplinare per assicurare lo standard GMP e il rilascio dei lotti. Sarai protagonista nel processo