25.09.24 | Vollzeit | Boudry | INTERIMANAnd distribution activities for clinical and commercial cell therapy apheresis material and finished product. You will carry out day-to-day logistics and warehousing tasks including deviation management for region EMEA and APAC and supports logistics projects and improvements initiatives. Main internal partners
Später ansehen24.09.24 | Vollzeit | Boudry | INTERIMANmanagement for region EMEA and APAC and supports logistics projects and improvements initiatives. Main internal partners are Scheduling & Logistics, Apheresis Operations, Manufacturing, Quality Assurance, Procurement and Technical Operations regionally and globally. Key external collaborators are specialty
Später ansehen24.09.24 | Vollzeit | Neuchâtel | CK GroupCK QLS are recruiting for a Computerized System Validation Specialist to join our client on a contract basis at their site in Neuchatel. START DATE ASAP/October 14th 2024 DURATION 12 months Duties The job holder is accountable for life cycle management activities of systems used in the QC
Später ansehen23.09.24 | Vollzeit | Boudry | JobLeads GmbH | CHF 100’000 - CHF 125’000 Individual contributing manager who support SCLT’s Operations Specialists managing real-time operational issues while maintaining a positive, inclusive, and professional team atmosphere and delivering on SCLT strategy - Manage Tier 1’s department (GPO) or regional cross-functional projects - Manage supply
Später ansehen23.09.24 | Vollzeit | Couvet | JobLeads GmbH | CHF 80’000 - CHF 100’000 Dossier managed by the Customer/Product Owner and also to support the site in the Company Regulatory Surveillance initiatives. The position holder is responsible to ensure the proper support of the GMP stakeholder regarding the Product's Dossier and the Regulatory Surveillance. As a member of the Quality
Später ansehen22.09.24 | Vollzeit | Couvet | JobLeads GmbH | CHF 80’000 - CHF 100’000 Dossier managed by the Customer/Product Owner. Additionally, it supports the site in the Company Regulatory Surveillance initiatives. The position holder is responsible for ensuring the proper support of the GMP stakeholder regarding the Product's Dossier and the Regulatory Surveillance. As a member
Später ansehen22.09.24 | Vollzeit | Neuchâtel | JobLeads GmbH | CHF 80’000 - CHF 100’000 And across the site. Language & IT Skills - Fluent in French and English (C1 written and spoken). - Proficiency in all aspects of standard IT tools. Key Skills, Abilities, and Competencies - Strong project management skills to support project delivery and operational readiness. - A proven ability to lead
Später ansehen22.09.24 | Vollzeit | Neuchâtel | JobLeads GmbH | CHF 80’000 - CHF 100’000 Laboratory systems - Experience with project management and/or leadership enabling cross functional engagement to deliver project goals and timelines - A thorough knowledge of DI requirements and standard regulations for cGMPs operations - Ability to identify and communicate risks in area of responsibility
Später ansehen21.09.24 | Vollzeit | Neuchâtel | JobLeads GmbH | CHF 80’000 - CHF 100’000 Computer System Validation Expert vacancy requiring profound English knowledge for a globally operating Neuchâtel based company in the Pharma sector. Your tasks - Managing system activities with a focus on Analytical Instrument Qualification and Computerized System Validation - Supporting the Data
Später ansehen21.09.24 | Vollzeit | Neuchâtel | JobLeads GmbH | CHF 80’000 - CHF 100’000 Computer System Validation Expert vacancy requiring profound English knowledge for a globally operating Neuchâtel based company in the Pharma sector. Your tasks - Managing system activities with a focus on Analytical Instrument Qualification and Computerized System Validation - Supporting the Data
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