Lavoro S You - Colleretto Giacosa

Work Your Magic with us!Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dre...

Work Your Magic with us!Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dre...

Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dr...

Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dr...

SummaryThe IT Site Business Partner for Technical Research and Development to be based in Ivrea, Italy captures IT demand, collaborates with IT functions, and supports the implementation of digital strategies at the Ivrea site. The role contributes to the Product Roadmap, supports global rollouts an...

SummarySupport 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 ba...

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...

We are seeking an experienced and detail-oriented Legal Counsel to support our legal department in ensuring compliance with regulations, managing contracts, and mitigating legal risks across the group. The successful candidate will play a crucial role in providing legal guidance on corporate matters...

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)...

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...

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 cost-effective, G...

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...