Pharmaceutical Compliance Specialist

About the Role:As the Manufacturing Deviation and GMP Documentation Lead, you will oversee the management of all activities related to GMP production documentation. This includes the critical review, approval, issuance, and maintenance of documentation in accordance with GDDP rules and cGMP compliance standards.Key Responsibilities:Guarantee production...

About the Role:As the GMP Compliance Documentation Lead, you will oversee the management of all activities related to GMP production documentation. This includes the critical review, approval, issuance, and maintenance of documentation in accordance with GDDP rules and cGMP compliance standards.Key Responsibilities:Guarantee production documentation critical...

About the Role:In the realm of production, effective management of documentation is crucial for ensuring compliance and excellence in production standards. As a subject-matter expert, overseeing production changes and conducting related risk assessments is a key responsibility. Moreover, leading projects that enhance production processes and continuous...

Job Title: Manufacturing Deviation and GMP Documentation LeadWe are seeking a highly skilled Manufacturing Deviation and GMP Documentation Lead to join our team at Takeda Pharmaceutical. As a key member of our quality assurance team, you will be responsible for ensuring the management of all activities related to GMP production documentation, including...

About the Role:As a Visual Inspection Lead at Takeda Pharmaceutical, you will be responsible for overseeing and managing activities within the scope of visual inspection. This includes coordinating and controlling these activities through the guidance of VI shift leaders, ensuring that all tasks are carried out in strict adherence to clearly defined...

Job Title: Quality Operations Excellence Specialist About the Role: We are seeking a Quality Operations Excellence Specialist to join our team at Takeda Pharmaceutical. As a key member of our Quality organization, you will play a critical role in promoting and driving strategic thinking and innovative approaches to change the business. Key...

Job SummaryWe are seeking a highly skilled Process Engineering Lead to join our team at Takeda Pharmaceutical. As a key member of our operations team, you will be responsible for ensuring the efficient and safe operation of our pharmaceutical manufacturing processes.Key ResponsibilitiesLead a team of process engineers and technicians to optimize and improve...

Job Title:Pharma Process Engineering LeadLocation: PisaJob Description:As a Pharma Process Engineering Lead, you will be responsible for ensuring the solid performance and efficiency of pharmaceutical machinery, aiming for operational excellence. You will lead a department, providing oversight to a high-skilled specialist or team of professionals working on...

About the Role:In the realm of production, management of documentation is crucial. This encompasses the creation, revision, and issuance of electronic Manufacturing Batch Records and Equipment Specifications, all in strict adherence to GDDP and cGMP standards. As a subject-matter expert, overseeing production changes and conducting related risk assessments...

About the Role:Takeda is seeking a highly skilled Production Specialist to oversee production documentation, manage change control, and ensure compliance with GMP regulations. The ideal candidate will have experience in aseptic production and a strong understanding of sterile manufacturing processes.Key Responsibilities:Develop, revise, and approve...

About the Role:Takeda is seeking a highly skilled Manufacturing Deviation and GMP Documentation Lead to join our team in Pisa, Italy.Job Summary:The Manufacturing Deviation and GMP Documentation Lead will be responsible for managing all activities related to GMP production documentation, including critical revision, approval, issuance, and maintenance...

About the Role:We are seeking a highly skilled Manufacturing Deviation and GMP Documentation Lead to oversee the management of all activities related to GMP production documentation. This includes critical review, approval, issuance, and maintenance of documentation in accordance with GDDP rules and cGMP compliance standards.Key Responsibilities:Guarantee...

About the RoleTakeda is seeking a skilled Project Coordinator to join our team in Pisa. As a key member of our production team, you will be responsible for managing documentation, ensuring compliance with GDDP and cGMP standards, and leading projects to enhance production processes.Key Responsibilities:Manage the creation, revision, and issuance of...

About the Role:As the Manufacturing Deviation and GMP Documentation Lead, you will oversee the management of all activities related to GMP production documentation. This includes the critical review, approval, issuance, and maintenance of documentation in accordance with GDDP rules and cGMP compliance standards. Additionally, you will be responsible for...

Job DescriptionAs a Maintenance Technician at Takeda Pharmaceutical, you will be responsible for executing corrective and preventive maintenance activities for GmP/non-GmP equipment/systems of the Pisa site. You will perform maintenance activities in accordance with EHS and GMP rules to maintain the site's equipment/systems in perfect condition.Key...

DescriptionJob Title: GMP Documentation SpecialistLocation: PisaEnsure GMP compliance through effective management of production documentation, including critical revision, approval, issuance, and maintenance.Develop and execute training programs on production documentation, focusing on strong training efficacy.Manage logistics for manufacturing and visual...

About the Role:As a Visual Inspection Lead at Takeda Pharmaceutical, you will oversee and manage activities within the scope of visual inspection, coordinating and controlling these through the guidance of VI Shift leaders. Your primary responsibility will be to ensure that all tasks are carried out in strict adherence to clearly defined operating...

About the Role:In the pharmaceutical industry, the effective management of documentation is crucial for production processes. As a subject-matter expert, the Production Specialist will oversee the creation, revision, and issuance of electronic Manufacturing Batch Records and Equipment Specifications, adhering to GDDP and cGMP standards.Main...

    About the RoleAs a Visual Inspection Lead at Takeda Pharmaceutical, your key responsibility will be overseeing and managing activities within your scope, ensuring the guidance of VI Shift leaders. Your role will be pivotal in guaranteeing that all tasks are carried out in strict adherence to clearly defined operating procedures, guaranteeing that...

About the Role:In the realm of pharmaceutical production, proper documentation management is crucial for maintaining quality and compliance. As a subject-matter expert, you will oversee production changes, conduct risk assessments, and lead projects to enhance production processes and continuous improvement initiatives.Your Key Responsibilities:Complete and...