24.07.24 | Vollzeit | Neuchâtel | Takeda PharmaceuticalAs across functions and business units. Directs organization of 4 to 5 direct reports (Managers) and approximately 70 indirect headcount. Manages overall coaching, training, development and succession plans for the team. Creates an environment that fosters lifelong learning and a growth mindset enabling
Später ansehen24.07.24 | Vollzeit | Neuchâtel | Takeda PharmaceuticalBy 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 Privacy Notice and Terms of Use . I further attest that all information I submit in my
Später ansehen24.07.24 | Vollzeit | Neuchâtel | Takeda PharmaceuticalTo act as Qualified Person Delegate. How you will contribute Ensures the day-to-day quality oversight of the Quality Control activities and Raw Material management related to his/her scope of responsibility Ensures raw material release and manages specifications Collaborates with suppliers to address
Später ansehen24.07.24 | Vollzeit | Neuchâtel | Takeda PharmaceuticalOf management and documents approval. Supervise the Quality Control laboratory activities to assure timely availability and accuracy of results. Ensure that all in-process samples, raw material and final products are analyzed in accordance with SOPs and regulatory requirements to applicable GMP’s and standards
Später ansehen24.07.24 | Vollzeit | Neuchâtel | Takeda PharmaceuticalDelivery of test results while upholding the highest standards of quality management practices. Additionally, you'll have the opportunity to step into a managerial capacity, providing backup support and contributing to the seamless flow of our quality assurance processes. If you're passionate about
Später ansehen24.07.24 | Vollzeit | Neuchâtel | Takeda PharmaceuticalEmployment application is true to the best of my knowledge. Job Description About the role As a Quality Systems Expert at our Neuchatel site, you will report to the Quality Systems Manager. Your responsibilities will include managing documentation and quality systems integration to align with Takeda's
Später ansehen17.07.24 | Vollzeit | Neuchâtel | Takeda PharmaceuticalDelivery of test results while upholding the highest standards of quality management practices. Additionally, you'll have the opportunity to step into a managerial capacity, providing backup support and contributing to the seamless flow of our quality assurance processes. If you're passionate about
Später ansehen16.07.24 | Vollzeit | Neuchâtel | Takeda PharmaceuticalOf management and documents approval. Supervise the Quality Control laboratory activities to assure timely availability and accuracy of results. Ensure that all in-process samples, raw material and final products are analyzed in accordance with SOPs and regulatory requirements to applicable GMP’s and standards
Später ansehen25.07.24 | Vollzeit | Neuchâtel | Takeda PharmaceuticalSystems (e.g. laboratory investigations, out-of- specification investigations, assay validation, management review, CAPA, and process control) that ensure products conform to defined requirements. - Understands and deploys processes to assure conformance to regulations. Actively leads or presents
Später ansehen15.07.24 | Vollzeit | Neuchâtel | Takeda PharmaceuticalBy 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 Privacy Notice and Terms of Use . I further attest that all information I submit in my
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