14.09.24 | Vollzeit, Teilzeit | Olten | jobs.alpiq.comCompliance Specialist (f/m/d) 80-100% Date 10 Sep 2024 Job ID 8712 Company Alpiq AG Location Olten, CH Contract Type Permanent Job Type Full-time position Job Level Experienced professionals LinkedIn #LI-SFCH Our Compliance team is managing compliance risks in a diversified business
Später ansehen07.09.24 | Vollzeit, Teilzeit | Olten | jobs.alpiq.comAnd compliance team in order to ensure proper governance and risk management. - Help us to further develop our future set up for becoming a leading renewables team in an
Später ansehen31.08.24 | Vollzeit, Teilzeit | Olten | jobs.alpiq.comM2M) data. - Ensure Compliance Oversee compliance quality within portfolios and lead User Acceptance Testing (UAT) for Energy Trading and Risk Management (ETRM) and reporting tools, ensuring they meet our rigorous standards. - Lead and Collaborate in Projects Play a crucial role in both internal
Später ansehen22.08.24 | Teilzeit | Solothurn | Ypsomed AGParticipation. Ypsomade. As a leading company in our industry, we have made a name for ourselves through continuous growth. Become part of our successful team of our System Verification & Product Support department and contribute your expertise. System Verification Manager - Mechanics 80 - 100% Ref
Später ansehen10.08.24 | Teilzeit, Vollzeit | Olten | jobs.alpiq.comBattery Energy Storage (BESS) Supply Chain Manager (f/m/d) Date 3 Sep 2024 Job ID 8680 Company Alpiq AG Location Olten, CH Contract Type Permanent Job Type Full-time position Job Level Experienced professionals LinkedIn #LI-SFCH Join us in shaping the future of Alpiq, where you'll play
Später ansehen27.07.24 | Vollzeit, Teilzeit | Olten | jobs.alpiq.comThis important asset being at the heart of this transformation. As Data Architect you play a crucial role in managing a company's data strategy, infrastructure, and systems. Your responsibilities span various aspects of data management, ensuring that data is accurately stored, processed, and made accessible
Später ansehen11.07.24 | Teilzeit | Solothurn | Ypsomed AGIn compliance with ISO 13485 and FDA Medical Device Design Control processes - Contribute to requirements definition, create design documentation and verification test plans - Participate in peer reviewing of the various hardware development artifacts - Support the verification team with HW related
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