Lavoro Quality - Lessona

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...

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...

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 responsible for timely p...

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...

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 responsible for timely ...

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, GxP and ...

Summary Location: Ivrea, Italy 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) in line with the overall CMC project development plan; ensure project specifi...

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...

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, GxP and ...

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, ...

Descrizione PropostaGruppo MIDI S.r.l., Società di Alta Formazione Professionale Certificata, seleziona massimo 20 partecipanti per un percorso formativo che crea professionisti specifici per il settore dei Dispositivi Medici e della Diagnostica in Vitro.Al termine di questo percorso formativo, il c...

PositionThe Quality Claims Manager is responsible for overseeing and optimizing the quality assurance processes related to claims management, developing and implementing strategies to ensure that claims are handled accurately, efficiently, and in compliance with regulatory requirements.Job Responsib...

Company descriptionTerry Soot Management Group (TSMG) is a field data collection company founded in 2017 in Europe. We collect data where automation is not possible. We count features, take pictures, make videos, record speech, and scan areas for every detail you need to make more informed decisions...

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...

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...