27.04.24 | Teilzeit, Vollzeit | Olten | jobs.alpiq.comWith the overall enterprise architecture strategy - Provide expert guidance and support to project teams on architectural matters, ensuring best practices are followed - Evaluate proposed solutions for technical viability and alignment with architectural standards and business objectives - Collaborate with other
Später ansehen20.04.24 | Teilzeit, Vollzeit | Olten | jobs.alpiq.comTo deliver on IT solutions for business - Work closely with department heads and the PMO team to develop the project management system, guidelines, standards, KPIs and
Später ansehen20.04.24 | Teilzeit, Vollzeit | Olten | jobs.alpiq.comStakeholder needs. This includes managing the relationship with the PPM Tool vendor Keto as well as with internal user group members. You ensure best practices around application management and will work closely with the Stakeholders following internal guidelines in Application and Change Management. Your
Später ansehen18.04.24 | Vollzeit | Oberdorf (BL) | Randstad Schweiz AGMeetings. - Provide guidance on requirements of QS processes to resources that execute these processes. - May be requested to participate in audit readiness activities, as well as assist
Später ansehen21.03.24 | Teilzeit | Solothurn | Ypsomed AGDevices sowie die dazugehörende technische Dokumentation gemäss ISO13485, MDR, CFR Part 820, produktspezifische Standards, nationale Guidelines und Gesetze für den gesamten Product Lifecycle im Verantwortungsbereich - Koordination und Bearbeitung von Change Control Projekten und Aufrechterhaltung
Später ansehen09.03.24 | Teilzeit, Vollzeit | Olten | jobs.alpiq.comAnd compliant with industry standards - Continuous improvement and refactoring of legacy components - Collaborating with cross-functional teams - Provide technical guidance and support to other team members - Stay up to date with the latest trends and technologies in software engineering - Ready to provide
Später ansehen29.02.24 | Teilzeit | Solothurn | Ypsomed AGOr Natural/Medical Sciences or equivalent experience - At least 4 years of professional experience in Regulatory Affairs with focus medical device - Expertise in Active Medical Devices related regulations and guidance documents in EU and US - Excellent organizational and people skills - Very good English
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