Lavoro Novartis - Saluggia

SummaryGuarantee the operation in compliance of all the pharmaceutical and general equipment and systems present in Saluggia site (intended GMP compliance, Normative and Standard compliance, eCompliance) in order to satisfy necessary requirements of pharmaceutical processes and safety requirements, ...

Summary Guarantee the operation in compliance of all the pharmaceutical and general equipment and systems present in Saluggia site (intended GMP compliance, Normative and Standard compliance, eCompliance) in order to satisfy necessary requirements of pharmaceutical processes and safety requirements,...

Summary Guarantee the operation in compliance of all the pharmaceutical and general equipment and systems present in Saluggia site (intended GMP compliance, Normative and Standard compliance, eCompliance) in order to satisfy necessary requirements of pharmaceutical processes and safety requirements,...

SummaryGuarantee the operation in compliance of all the pharmaceutical and general equipment and systems present in Saluggia site (intended GMP compliance, Normative and Standard compliance, eCompliance) in order to satisfy necessary requirements of pharmaceutical processes and safety requirements, ...

Responsible for developing, implementing and managing the site performance qualifications and requalification of existing equipment and cycles as well as any new equipment. Responsible for developing, implementing and managing the site process validation, primary packaging validation, process perfor...

Job Description SummaryGuarantee the operation in compliance of all the pharmaceutical end general equipment and systems present in Saluggia site (intended GMP compliance, Guarantee the operation in compliance of all the pharmaceutical end general equipment and systems present in Saluggia site (inte...

Responsible for developing, implementing and managing the site performance qualifications and requalification of existing equipment and cycles as well as any new equipment. Responsible for developing, implementing and managing the site process validation, primary packaging validation, process perfor...

Responsible for developing, implementing and managing the site performance qualifications and requalification of existing equipment and cycles as well as any new equipment. Responsible for developing, implementing and managing the site process validation, primary packaging validation, process perfor...

Job Description SummaryResponsible for developing, implementing and managing the site performance qualifications and requalification of existing equipment and cycles as well any new equipment. Responsible for developing, implementing and managing the site process validation, primary packaging valida...

Responsible for developing, implementing and managing the site performance qualifications and requalification of existing equipment and cycles as well as any new equipment. Responsible for developing, implementing and managing the site process validation, primary packaging validation, process perfor...

RLT Analytical Product Project Leader (m/f/d) Job ID: REQ-10015150Jul 11, 2024Location: Ivrea, ItalySummary Role Purpose: Define, lead and manage the analytical project strategy including the overall analytical control strategy for Drug Substance(s) and radiopharmaceutical parenteral Drug Product(s)...

The MBR Designer plays a pivotal role in supporting Manufacturing Execution Systems (MES) operating sites by providing expert design and business process support. This role is responsible for the delivery and updating of Master Batch Record (MBR) Design Elements, ensuring alignment with global core ...

Summary Create and drive with scientific & technological excellence the formulation development in close collaboration with operations, analytics, engineering and relevant SMEs, QA and the project DPPL. Development activities include among others: formulation and process-design, control strategy, qu...

The MBR Designer plays a pivotal role in supporting Manufacturing Execution Systems (MES) operating sites by providing expert design and business process support. This role is responsible for the delivery and updating of Master Batch Record (MBR) Design Elements, ensuring alignment with global core ...

SummaryCapo turno IIIl capo turno è responsabile della gestione del suo team per eseguire le operazioni di produzione secondo il programma in conformità con le regole HSE e GMP.Esperto di processoFornire supporto tecnico e scientifico in prima linea per tutte le questioni specifiche del processo per...