16.09.24 | Vollzeit | Yverdon-les-Bains | JobLeads GmbH | CHF 80’000 - CHF 100’000 Which will be used to prepare the related registration documentation. - Author or review routine validation protocols and reports, associated change controls and support execution at the shop floor. - Lead and drive investigations for validation-related matters and implement corrective and preventive
Später ansehen15.09.24 | Vollzeit | Lausanne | JobLeads GmbH | CHF 125’000 - CHF 150’000 Including at least 3 years within Clinical Quality Management System & Compliance. 3. Experience in managing and conducting GCP audits (CROs, TMF, Investigational Sites and CSR). 4. Excellence knowledge of GCP. Current and strong working knowledge of GCP, CFR Title 21 and regulatory guidance’s including
Später ansehen31.08.24 | Vollzeit | Gland | JobLeads GmbH | CHF 80’000 - CHF 100’000 And DVP) - Migrations - Processing of physical shares - Shareholder register - Investigation on any transfers related issue (reconciliation-s breaks) - Front-office/Customer Care support - Daily contacts and monitoring with counterparts and custodians - Daily usage of SWIFT messages MT54 - Usage
Später ansehen25.08.24 | Vollzeit | Lausanne | JobLeads GmbH | CHF 125’000 - CHF 150’000 Management System & Compliance - Experience in managing and conducting GCP audits (CROs, TMF, Investigational Sites and CSR) - Excellence knowledge of GCP. Current and strong working knowledge of GCP, CFR Title 21 and regulatory guidance's including, ICH quality, clinical, multidisciplinary guidance
Später ansehen24.08.24 | Vollzeit | Gland | JobLeads GmbH | CHF 80’000 - CHF 100’000 To the whole organization (such as case investigation, process and workflow improvement, chargebacks and dispute claim with Fraud Monitoring team etc.) - Drive and support the automation in our internal tools for card management activity - Business monitoring of the performance of the services, invoice
Später ansehen12.08.24 | Vollzeit | Grens | JobLeads GmbH | CHF 80’000 - CHF 100’000 For medical devices and preparing clinical data documents that support regulatory submissions for the EU, US, and other international markets. The Medical Writer also assists with writing and reviewing regulatory documents related to the preparation, conduct and reporting of clinical investigations and other
Später ansehen26.08.24 | Vollzeit | Corsier-sur-Vevey | Randstad Schweiz AGinvestigations.) - Participating in maintaining the functionality of the laboratories/clean rooms - Interacting with different stakeholders (e.g. Quality Assurance, Project Managers, or Operational team) - Participate in local improvement projects related to the support and sampling activities Your profile
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