Lavoro Support English - Colleretto Giacosa

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...

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 ...

SummaryLocation: Ivrea, ItalyRole PurposeDefine, 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 specific h...

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 ...

Major AccountabilitiesEnsure that raw materials used for the manufacturing process are always available in the right amount and properly stored according to their status.Support Production Manager to write down and validate the Standard Operating Procedures and Work Instructions relating to producti...

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...

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...

Major Accountabilities Ensure that raw materials used for the manufacturing process are always available in the right amount and properly stored according to their status. Support Production Manager to write down and validate the Standard Operating Procedures and Work Instructions relating to produc...

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, ...

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...

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...

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...

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 Create 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, qu...