27.05.24 | Vollzeit | Neuchâtel | RM Group AGstandards to uphold operational excellence - Leading the design, qualification, and implementation of equipment and plant optimizations - Monitoring and approving the implementation of supplier interventions for facility and utility equipment - Facilitating cross-functional collaboration to enhance
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 PharmaceuticalSafety, report risk situations and improvement opportunities to supervisory personnel. Deviations Lead or approve “deviations” with in line with to standard procedures and regulatory requirements. Support all investigations (intersites and all kind of criticity of deviations) related to deviations
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 | RM Group AGstandards to uphold operational excellence - Leading the design, qualification, and implementation of equipment and plant optimizations - Monitoring and approving the implementation of supplier interventions for facility and utility equipment - Facilitating cross-functional collaboration to enhance
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 PharmaceuticalSafety, report risk situations and improvement opportunities to supervisory personnel. Deviations Lead or approve “deviations” with in line with to standard procedures and regulatory requirements. Support all investigations (intersites and all kind of criticity of deviations) related to deviations
Später ansehen08.05.24 | Vollzeit | Neuchâtel | RM Group AGAnd processes, ensuring alignment with regulatory standards and internal requirements - Executing validation activities, including IQ, OQ, PQ, test method validation, and process validation, utilizing appropriate tools and methodologies - Analyzing validation data and providing insights to optimizing product
Später ansehen14.05.24 | Vollzeit | Neuchâtel | Randstad Schweiz AG% - Working hours standard This resource will be specifically responsible for the following tasks - Review deviations in the framework of engineering events within quality systems (i.e. Trackwise) to verify acceptability and adherence to standard procedures and regulatory requirements. This includes
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