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Zizers

    Quality Manager, Innovation Translation Center - Zizers, Schweiz - AO Foundation

    AO Foundation
    AO Foundation Zizers, Schweiz

    Gefunden in: Jobcloud CH C2 - vor 2 Tagen

    AO Foundation background
    Beschreibung
    Job Facts
    • For this role, we are open to offer a job-sharing model (e.g.: 50% / 50%). If you prefer this option, please indicate it in your application.
    • Work location: Zizers /Landquart (1h commute with train from Zürich HB)
    • Hybrid work model: 2-3 days/week in the office required
    Main Requirements

    Education

    • BSc preferably in natural science or similar
    • Education as "Qualitätsmanagement Beauftragter TüV" or similar

    Job specification

    • Ability to develop and manage a quality management system in compliance with regulatory requirements
    • Knowledgeable about ICH E6 and ISO 14155 and regulatory requirements (Swiss, and basic knowledge about EU, USA)
    • Ability to scout for regulatory updates and updates of ICH guidelines and ISO standards
    • Ability to work both, independently and in a team and to communicate effectively
    • Proficiency using MS Office including Word, Excel, PowerPoint
    • Ability to work in a document management system and/or to use other QMS IT systems
    • Strong written and oral communication skills in German and English
    • Ability to perform internal Quality Control of projects
    • Preferably ability to perform Audits internal and external (if trained to do so)
    • Teaching skills to train employees and vendors on QMS and regulatory updates
    Main Responsibilities

    In general (QMS)

    • Maintenance, implementation, inspection, and continuous improvement of AO ITC Clinical Evidence quality management system
    • Ensure alignment of the top management with the QMS (business requirements in accordance with relevant regulations)
    • Review, revise and maintain quality documents vs. ISO 9001 standards (ie ISO 14155), ICH guidelines and applicable regulations
    • Develop new processes in collaboration with process owner and provide expertise for process development and documentation

    In general (regulatory compliance)

    • Scout for new and/or revised regulations (Switzerland, EU, USA, any other country as required based on operational activities)
    • Scout for new and/or revised standards and norms (ISO, ICH)

    Education of employees

    • Ensure compliant introduction of new employees in collaboration with the AO HR and the assigned line manager
    • Ensure (and perform) adequate training (introduction and continuous) in the QMS, regulations and guidelines
    • Ensure the Function and Competency profiles are in line with the QMS and organizational chart(s) of the organization
    • Ensure documentation of external and internal continuous education of the employees in accordance with the QMS
    • Ensure the CVs of the employees are available in accordance with the QMS
    • Ensure the specific needs as defined in the AO ITC Clinical Evidence QMS are aligned with the AO Foundation HR
    • Ensure correct hand-over and documentation for leaving employees (in alignment with the AO Foundation HR)

    External collaborators (vendors)

    • Support Manager Clinical Services in ensuring adequate training of contracted staff (vendors)
    • Support Manager Clinical Services in quality control and quality assurance activities of contracted staff (vendors)

    Quality control and quality assurance

    • Plan, execute and follow-up internal quality control activities (internal project audits) according to the QMS
    • Plan, execute (if competent) and follow-up audits of investigation sites and vendors (in collaboration with the Manager Clinical Services) according to the QMS
    • Ensure that CAPA from any of the above activities are performed and resolved adequately

    Quality control and quality assurance performed by external stakeholders (authorities, sponsors)

    • Coordinate and lead the announced audits internally
    • Be the primary communication partner to external auditor
    • Inform the top management about announcement, performance and CAPA of any external audit
    • Perform the CAPA
    • Support audits performed by authorities or sponsor at investigation clinics managed by AO ITC Clinical Evidence as required


    Working for us, you can expect:

    • An interesting and varied job in an exciting and innovative organization
    • The opportunity to be part of a highly committed international team
    • Modern infrastructure
    • Employment conditions which match the requirements and offer a high degree of flexibility regarding working hours and location

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