![Ordinato per](/assets/img/filtry.png)
Lavoro Quality - Biella
46-60 z 84 offerte di lavoroQC Technician (fixed-term)
![NOVARTIS](/assets/img/company.png)
SummaryThe QC Technician performs the analysis on batches and incoming materials according to cGMP rules and SOPs.About The RoleMajor accountabilities:Perform the analysis of batches following specific training;Promptly report to the Quality Control Supervisor and the Qualified Person any deviation ...
![11.02.2025](/assets/img/time.png)
QC Technician (fixed-term)
![NOVARTIS](/assets/img/company.png)
Summary The QC Technician performs the analysis on batches and incoming materials according to cGMP rules and SOPs. About The Role Major accountabilities: Perform the analysis of batches following specific training; Promptly report to the Quality Control Supervisor and the Qualified Person any devia...
![11.02.2025](/assets/img/time.png)
Clinical Trial Supply Manager
![NOVARTIS ACC](/assets/img/company.png)
Summary Clinical Trial Supply Manager (CTSM) defines and executes an optimal clinical trial supply strategy for a clinical trial including effective risk management to ensure supply continuity to patients. The CTSM is the GCS single point of contact at trial level for the integrated CTT (Clinical Tr...
![11.02.2025](/assets/img/time.png)
QC Technician (fixed-term)
![NOVARTIS ACC](/assets/img/company.png)
SummaryThe QC Technician performs the analysis on batches and incoming materials according to cGMP rules and SOPs.About The RoleMajor accountabilities:Perform the analysis of batches following specific training;Promptly report to the Quality Control Supervisor and the Qualified Person any deviation ...
![11.02.2025](/assets/img/time.png)
Clinical Trial Supply Manager
![NOVARTIS ACC](/assets/img/company.png)
SummaryClinical Trial Supply Manager (CTSM) defines and executes an optimal clinical trial supply strategy for a clinical trial including effective risk management to ensure supply continuity to patients.The CTSM is the GCS single point of contact at trial level for the integrated CTT (Clinical Tria...
![11.02.2025](/assets/img/time.png)
Pilot Plant Production Supervisor
![NOVARTIS PHARMA SCHWEIZ](/assets/img/company.png)
Support Production Manager to ensure the running of a production shift team such that the manufacturing program is achieved efficiently within the framework of regulatory compliance and operating within high standards of GMP, HSE, environmental protection and good working practices. Act as backup of...
![11.02.2025](/assets/img/time.png)
Pilot Plant Production Supervisor
![NOVARTIS PHARMA SCHWEIZ](/assets/img/company.png)
Support Production Manager to ensure the running of a production shift team such that the manufacturing program is achieved efficiently within the framework of regulatory compliance and operating within high standards of GMP, HSE, environmental protection and good working practices. Act as backup of...
![10.02.2025](/assets/img/time.png)
Pilot Plant Production Supervisor
![NOVARTIS ACC](/assets/img/company.png)
Summary Support Production Manager to ensure the running of a production shift team such that the manufacturing program is achieved efficiently within the framework of regulatory compliance and operating within high standards of GMP, HSE, environmental protection and good working practices. Act as b...
![10.02.2025](/assets/img/time.png)
QC Technician (fixed-term)
![NOVARTIS ACC](/assets/img/company.png)
Summary The QC Technician performs the analysis on batches and incoming materials according to cGMP rules and SOPs. About The Role Major accountabilities: Perform the analysis of batches following specific training; Promptly report to the Quality Control Supervisor and the Qualified Person any devia...
![10.02.2025](/assets/img/time.png)
TRD Pilot Plant Automation Engineer
![NOVARTIS ACC](/assets/img/company.png)
Summary Leads the Pilot Plant Automation function, which is responsible to establish, maintain and improve the automation processes with respect to site buildings, equipment and utilities. He coordinates all automation projects and initiatives, external vendors included. He provides cost-effective, ...
![10.02.2025](/assets/img/time.png)
Mass Spectrometry Expert (m/f/d)
![NOVARTIS ACC](/assets/img/company.png)
Summary Location: Ivrea, Italy Role Purpose Design, plan and perform Mass Spectrometry experiments as well as report and interpret results/outcome in line with the overall TRD RLT (Radioligand Therapy) project strategy for RLT Drug Substance(s) and Drug Product(s) in development. Ensure project know...
![10.02.2025](/assets/img/time.png)
TRD Pilot Plant Automation Engineer
![HEALTHCARE BUSINESSWOMEN’S ASSOCIATION](/assets/img/company.png)
Job Description SummaryLeads the Pilot Plant Automation function, which is responsible to establish, maintain and improve the automation processes with respect to site buildings, equipment and utilities. He coordinates all automation projects and initiatives, external vendors included. He provides c...
![10.02.2025](/assets/img/time.png)
TRD Pilot Plant CQV Engineer
![HEALTHCARE BUSINESSWOMEN’S ASSOCIATION](/assets/img/company.png)
Job Description SummaryThe CQV (Commissioning, Qualification and Validation) Engineer provides the Pilot Plant with Subject Matter Expert (SME) knowledge and skills related to commissioning, qualification and validation activities and requirements of facility, utilities and equipment. He is responsi...
![10.02.2025](/assets/img/time.png)
RLT Formulation Project Leader
![NOVARTIS](/assets/img/company.png)
SummaryCreate 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, qua...
![10.02.2025](/assets/img/time.png)
QC Technician
![NOVARTIS SOUTH AFRICA](/assets/img/company.png)
Summary The QC Technician performs the analysis on batches and incoming materials according to cGMP rules and SOPs. About The Role Major accountabilities: Perform the analysis of batches following specific training; Promptly report to the Quality Control Supervisor and the Qualified Person any devia...
![10.02.2025](/assets/img/time.png)
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