06.06.24 | Vollzeit | Neuchâtel | Takeda PharmaceuticalYou 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 and Manage
Später ansehen04.06.24 | 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 ansehen04.06.24 | 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 ansehen04.06.24 | 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 ansehen14.05.24 | Vollzeit | Neuchâtel | RandstadAnd software access management according to Takeda policies Other tasks related to conventional quality oversight might be occasionally requested to support the team (e.g. continuous improvement initiatives, GMP tour of technical area, etc.) The above-mentioned tasks are site-based, an on-site presence
Später ansehen14.05.24 | Vollzeit | Neuchâtel | Randstad Schweiz AGTraining and software access management according to Takeda policies - Other tasks related to conventional quality oversight might be occasionally requested to support the team (e.g. continuous improvement initiatives, GMP tour of technical area, etc.) The above-mentioned tasks are site-based, an on-site
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