Lavoro Health Technology Products - Ivrea

Key Responsibilities Perform 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 Qual...

SummaryAs a Micro QC Expert, you will be in charge of the execution and documentation of biological and microbiological testing in conformity to GMP standards and SOPs. Maintenance of the Micro laboratory compliance status and resolution of compliance-related issues. Competency in core activities of...

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...

SummaryThe Pilot Plant Manufacturing Team Head is responsible to establish and manage the Production unit and ensures the manufacturing program is achieved efficiently within the framework of regulatory compliance and operating within high standards of GMP, HSE, environmental protection and good wor...

Summary As a Micro QC Expert, you will be in charge of the execution and documentation of biological and microbiological testing in conformity to GMP standards and SOPs. Maintenance of the Micro laboratory compliance status and resolution of compliance-related issues. Competency in core activities o...

SummaryLocation: Ivrea, ItalyRole PurposeLeads and manages all Drug Product (DP) project activities linked to the development of radiopharmaceutical parenterals (both ready to use and freeze dried products). Supports & coaches team members, participates in scientific teams and contributes to the ove...

Summary The Pilot Plant Manufacturing Team Head is responsible to establish and manage the Production unit and ensures the manufacturing program is achieved efficiently within the framework of regulatory compliance and operating within high standards of GMP, HSE, environmental protection and good wo...

Summary Location: Ivrea, Italy Role Purpose Leads and manages all Drug Product (DP) project activities linked to the development of radiopharmaceutical parenterals (both ready to use and freeze dried products). Supports & coaches team members, participates in scientific teams and contributes to the ...