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p By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s a target="_blank" Privacy Notice /a and a target="_blank" Terms of Use /a. I further attest that all information I submit in my employment application is true to the best of my knowledge. /p h2bJob Description /b /h2 pSince 1972, Takeda has had two sites in Italy for producing plasma-derived drugs in Rieti and Pisa, supporting patients with rare and complex diseases. These sites focus on the production of therapies derived from immunoglobulins, albumin, and coagulation factors. As a partner of the National Health System, we transform plasma into life-saving drugs under the “National Self-Sufficiency of Blood and its Products” program. We provide high-quality drugs worldwide, with a strong presence in Europe, America, and Asia. /ppppp pAcross Italy and the world, Takeda is recognized as a Top Employer by the Top Employers Institute based on our commitment to career development, inclusion, learning, sustainability, wellness, and, most importantly, our values. /p pJoin us to make a difference. /p /p /p /p /ppbiOBJECTIVES/PURPOSE: /i /b /pullipManage the activities related to Process Improvement Stewardship Team  /p /lilipLead process improvement initiatives, monitoring, and stewardship /p /lilipProvide technical support about manufacturing processes, investigations, optimization, yield improvement projects, cycle time reduction  /p /li /ul pbiACCOUNTABILITIES: /i /b /pullipManage and coordinate the Process Improvement team, ensuring that all team members are aligned with business objectives and operate efficiently /p /lilipLead process improvement initiatives, monitoring, and stewardship /p /lilipProvide technical support about manufacturing processes, investigations, optimization, yield improvement projects, cycle time reduction, process robustness, Technology Transfer /p /lilipOversee product and process investigations, product impact assessment, risk assessment /p /lilipCollaborate with all other departments to ensure an integrated and cohesive approach /p /lilipEnsure compliance with regulations and quality standards, keeping Quality by Design documents up to date /p /lilipManage process validation strategy /p /lilipSupport the preparation of regulatory submission / meetings /p /lilipSupport regulatory inspections and defending technical decisions to regulatory agencies /p /li /ul pbiCORE ELEMENTS RELATED TO THIS ROLE: /i /b /pullipExcellent leadership and team management skills /p /lilipStrong strategic orientation and analytical thinking ability /p /lilipExcellent communication, collaboration and influencing skills /p /lilipExperience in managing complex projects and implementing innovative technologies /p /lilipAbility to anticipate changes and solve complex problems /p /lilipProject management skills and results orientation /p /lilipDevelopment of the team, providing strategic direction and support in complex scenarios /p /lilipDevelopment of strategic plans for departmental growth and operational efficiency /p /li /ul pbiDIMENSIONS AND ASPECTS - REQUIREMENTS: /i /b /p pbuTechnical/Functional (Line) Expertise /u /b /pullipMaster or PhD degree in technical/scientific education, preferably pharmaceutical sciences, chemistry, biotechnology, bioinformatics or pharma - process engineering /p /lilip5/7 previous experience in Leadership Role /p /lilipPrevious experience in plasma fractionation processes (Ideal - Preferred) or in biotechnology field knowledge of proteins Knowledge of GMP/GDP (mandatory) /p /lilipExperience in Process Validation (Preferred) /p /lilipExperienced in process optimization, capable of implementing strategies to enhance productivity /p /lilipProficient in continuous improvement processes /p /lilipProven experience in statistics, data analysis or equivalent academic experience/course record /p /lilipProven knowledge of six-sigma and DMAIC methodology  /p /lilipExcellent knowledge of Italian and English, both written and spoken - Fluent level /p /li /ul pbuLeadership /u /b /pullipFocuses on the few priorities and delivers superior results  /p /lilipElevates the capabilities of the organization for now and the future  /p /lilipStrategic enterprise thinking, finding innovative ways to serve patients build reputation and trust /p /lilipGood understanding of industry, scientific trends and market conditions to develop solutions enhancing compliance and quality of life for patients /p /lilipOrganizational skills /p /lilipGood communication and presentation skills as well as influencing skills /p /li /ul pbuDecision-making and Autonomy /u /b /pullipCreating the environment that inspires and enables people /p /lilipCreates clarity, fostering alignment and accountability /p /lilipIs courageous in making decisions based on sound business judgment or appropriately escalate topics with high criticality /p /li /ul pbiADDITIONAL INFORMATION: /i /b /pullipWillingness to travel to various internal/external Takeda meetings and events /p /li /ul h1bWhat Takeda can offer you: /b /h1pWe want our employees to succeed in everything they do - at work, at home, and in the community. This is why we offer world-class benefits and access to resources that can support people. /p pbHealth and Finance /b /pullipHealth Care Assistance Insurance /p /lilipEmployee Stock Purchase Plan /p /lilipEmployee discount programs on commercial establishments, shops, medical services /p /li /ul pbTraining and Development /b /pullipTechnical skill training and professional development /p /lilipJob Rotation programs for working in other departments /p /lilipSpontaneous employee groups for awareness on Diversity, Equity, and Inclusion issues and community engagement activities /p /lilipValue-based culture /p /li /ul pbIndividual Support /b /pullipWellness programs /p /lilipOn-site cafeteria and bar /p /lilipResources for mental, physical, financial, and spiritual health /p /lilipParental Leave /p /li /ul pbNOTE: /b /pullipbBelonging to protected categories (Law No. 68/99) will be considered a preferential qualification. /b /p /li /ul h1Important Considerations: /h1pAt Takeda, our patients rely on us to create quality products, and we aim to create a safe environment for our team members. As a result, we must follow strict rules in our manufacturing facilities to ensure we are not endangering the quality of the product or putting anyone at the site in harm's way. In this role, you may: /pullipWork in a controlled environment requiring special gowning and wearing protective clothing. /p /lilipNeed to remove all make-up, jewelry, contact lenses, nail polish, and/or artificial fingernails while in the manufacturing environment. /p /li /ul h1More About Us: /h1pAt Takeda, we are transforming patient care through the development of innovative specialty medicines and first-class patient support programs. Takeda is a patient-oriented company that will inspire and empower you to grow through life-changing work. /p pCertified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and aims for excellence in everything we do. We promote an inclusive and collaborative work environment where our teams are united by an unwavering commitment to delivering Better Health and a Brighter Future to people worldwide. /p h1Empowering our people to shine: /h1pTakeda is proud of its commitment to creating a diverse workforce and offering equal employment opportunities to all employees and applicants without distinction of race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information, marital status, or any other characteristic protected by law. /p p#GMSGQ /pp#LI-LA1 /p h2bLocations /b /h2ITA - Rieti h2bWorker Type /b /h2Employee h2bWorker Sub-Type /b /h2Regular h2bTime Type /b /h2Full time