07.05.25 | Vollzeit | Cressier (NE) | RandstadDiscrepancies(delivery delays, pricing issues, stockouts) to guarantee on-timeand complete deliveries. Utilize reports to foresee and addresspotential delivery/production delays. Ensure proper follow-up onquality concerns. - Maintainclear and timely communication regarding order processing,procedures
Später ansehen07.05.25 | Vollzeit | Bevaix | JobLeads GmbH | CHF 100’000 - CHF 125’000 Leadership team as well as a partner with the plant leadership teams to delivery the overall HR Experience. RESPONSIBILITIES AND DUTIES Strategic HR Advisor to all functional leadership- Coach and Advisor to managers, leaders and HR partners. - Working closely with other HR functions (HR services, Total
Später ansehen04.05.25 | Vollzeit | Boudry | JobLeads GmbH | CHF 80’000 - CHF 100’000 Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more
Später ansehen01.05.25 | Vollzeit | Yverdon-les-Bains | JobLeads GmbH | CHF 80’000 - CHF 100’000 S4 HANA and different modules like MM, PP, ALM, SQL, reporting - Analytics, SD modules in Pharma Industry, SharePoint, MS office, Project management, Service Now. - Highest experience in planning & logistics Supply Chain processes as well as working with all functional workstreams required
Später ansehen15.04.25 | Vollzeit | Marin-Epagnier | JobLeads GmbH | CHF 80’000 - CHF 100’000 Process Development, Business Units and Technical Services teams - Define, own, deploy and communicate the department’s priorities in line with EM FAB strategy - Drive technical comparisons and analysis with benchmark companies and manage EM wafer foundries management Profil - Engineering degree
Später ansehen12.04.25 | Vollzeit | Neuchâtel | JobLeads GmbH | CHF 80’000 - CHF 100’000 QA Validation Consultant to join our teams in Neuchatel. Responsibilities - Review of validation protocols - Assess validation protocols related to equipment, processes, CIP, SIP, computerized systems, and HVAC/Utilities. - Ensure compliance with GMP requirements, internal company standards
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