Lavoro S You - Lessona

Job Description Summary The QC Technician performs the analysis on batches and incoming materials according to cGMP rules and SOPs. Job Description Major accountabilities: Perform the analysis of batches following specific training. Promptly report to the Quality Control Supervisor and the Qualified...

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...

Key ResponsibilitiesPerform Micro / EM analysis of batches according to internal SOPs;Execute process validation protocols, method validation protocols and every study tied to drug products involved in technology transfer for the field of expertise.Promptly report to Quality Control Head and Qualifi...

Role purpose:As Single RAN Access system Engineer you will be part of the global Mobile Access Engineering organization unit that aims to deliver the superiority of our Mobile Network design by the best and most innovative design, engineering and optimisation and implementation across Vodafone.You w...

RLT Analytical Product Project Leader (m/f/d)Job ID: REQ-10015150Jul 11, 2024Location: Ivrea, ItalySummaryRole 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) i...

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, quali...

The 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 responsible for timely planning...

Job Description SummaryThe QC Technician performs the analysis on batches and incoming materials according to cGMP rules and SOPs.Job DescriptionMajor accountabilities:Perform the analysis of batches following specific training.Promptly report to the Quality Control Supervisor and the Qualified Pers...

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...

We are seeking an experienced and visionary Global Application Manager to oversee various Application Managers and contribute significantly to the overall enterprise architecture and IT strategy of our company. The successful candidate will play a crucial role in ensuring the alignment of applicatio...

Major AccountabilitiesPerform the analysis of batches following specific training.Promptly report to the Quality Control Supervisor and the Qualified Person any deviation and/or out of specification detected during the analysis activities.Collaborate with the Quality Control Head/supervisor for the ...

SummaryLocation: Colleretto GiacosaRole PurposeResponsible to ensure compliance to cGxP standards for topics within the area of responsibility (during development, transfer, release, and stability), including safety testing, monitoring, and trending. Provide guidance, support, and leadership for imp...

Job Description Summary The 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 respons...

Job Description SummaryThe Production Supervisor supports the 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 p...

SummaryThe 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 ...