28.05.24 | Vollzeit | Neuchâtel | Takeda PharmaceuticalOversight and quality assurance (QA) support to partners (QA, manufacturing, projects). They actively participates to internal and external inspections. How you will contribute Quality Management of Systems Follow and implement changes in project/process or operational mode, depending on the perimeter
Später ansehen25.05.24 | Vollzeit | Neuchâtel | Takeda PharmaceuticalIn Neuchâtel (clinical phase III and commercial). Manage/prepare the necessary supportive documentation for regulatory submissions and for major change projects in Neuchâtel facility. Prepare/Review documentation for change controls, audit observations and regulatory agency questions. Support/Write
Später ansehen25.05.24 | Vollzeit | Neuchâtel | Takeda PharmaceuticalInspection Process You will ensure Compliance with Takeda Quality Management System, regulations and standards, manage Compliance Risk Assessments and represnet your department during regulatory inspections. Ensure the oversite of Quality Systems Pocesses. You will lead a permanent Inspection ready status
Später ansehen25.05.24 | Vollzeit | Neuchâtel | Takeda PharmaceuticalOf internal management as well as 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. C reates an environment that fosters lifelong learning
Später ansehen25.05.24 | 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 ansehen27.05.24 | Vollzeit | Neuchâtel | Takeda PharmaceuticalIn Neuchâtel (clinical phase III and commercial). Manage/prepare the necessary supportive documentation for regulatory submissions and for major change projects in Neuchâtel facility. Prepare/Review documentation for change controls, audit observations and regulatory agency questions. Support/Write
Später ansehen25.05.24 | 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 ansehen25.05.24 | Vollzeit | Neuchâtel | Takeda PharmaceuticalInspection Process You will ensure Compliance with Takeda Quality Management System, regulations and standards, manage Compliance Risk Assessments and represnet your department during regulatory inspections. Ensure the oversite of Quality Systems Pocesses. You will lead a permanent Inspection ready status
Später ansehen25.05.24 | Vollzeit | Neuchâtel | Takeda PharmaceuticalThrough GMP audits or events management). Responsible for quality aspects during the validation activities (routine and projects). Shall promote and be involved in Continuous Improvement. Understand and apply Takeda EHS (Environment, Health, Safety) guidelines and commitments policy, take care of its own
Später ansehen07.05.24 | Vollzeit | Neuchâtel | RMIT Professional Resources AGSystems management and data integrity- Conducting environmental sampling of production areasYour experience/knowledge- 2+ years of experience in a QC microbiology laboratory in the pharmaceutical industry or a similar field of activity- Profound knowledge of microbiology testing and analysis conducted
Später ansehenVerpassen Sie nie wieder einen passenden Job!
Alle Jobs für Information Manager in Neuchâtel Kanton kostenlos abonnieren.