Stellenangebote für Quality Management Jobs in Basel

quality products to patients. The group excels in its work through innovation, teamwork, dedication, and mutual respect and contributes every day, continuously improving what it does. In “Europe Biologics“ (PTDE), we support biologics from Phase I into the Market. Our activities encompass process

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Vergleichbaren Fachrichtung � Mind. 5 Jahre Berufserfahrung im Bereich IT Compliance � Umfangreiche Kenntnisse im Bereich IT Compliance im GxP-relevanten Umfeld (z.B. ITIL, COBIT, CMMI), im IT Process/Project Quality Management oder in Computer System Validierung (GAMP) � Fundierte Kenntnisse von regulatorischen

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Decision and action, we believe that good business means a better world. Pharma Technical Development (PTD) delivers the pipeline while efficiently transforming scientific ideas into products. PTD is responsible to develop innovative technical solutions to supply quality products to patients within

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23.04.18 | Vollzeit | Schweiz | 80.000 - 100.000

Combination of strong coordination skills as well as digital expertise and stakeholder management. A successful candidate will successfully guide multiple content providers and work with creative teams in order to deliver high quality digital multichannel content that meets business objectives, is consistent

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22.04.18 | Vollzeit | Schweiz Vereinigte Staaten | 60.000 - 80.000

Analytics and audits, the direction offered from this position must support the business on a global level, delivering to senior management quality assurance strategies that enable faster and more confident product ing internal teams, customers and stakeholders to excellent levels of

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20.04.18 | Vollzeit | Schweiz

Combination of strong coordination skills as well as digital expertise and stakeholder management. A successful candidate will successfully guide multiple content providers and work with creative teams in order to deliver high quality digital multichannel content that meets business objectives, is consistent

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CTRi Project was established to serve two business needs1) The need to be compliant with the new Clinical Trial Regulation (CTR) being implemented to replace the current Clinical Trial Directive (CTD)2) The need to improve the efficiency and effectiveness of study start up and management and

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20.04.18 | Vollzeit | Schweiz | 100.000 - 125.000

Destination email* Powered By ChronoForms Business Analyst Clinical Trial Systems Basel Ref. 9598 Contract position Client's sector Healthcare, Pharma & Chemistry Skills CTRi, BA, Clinical, Data quality Required languages English Industry Information Technology For our client, a leading

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20.04.18 | Vollzeit | Schweiz | 125.000 - 150.000

CTRi Project was established to serve two business needs1) The need to be compliant with the new Clinical Trial Regulation (CTR) being implemented to replace the current Clinical Trial Directive (CTD)2) The need to improve the efficiency and effectiveness of study start up and management and

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20.04.18 | Vollzeit | Schweiz | 80.000 - 100.000

We are looking for someone to join as an International Clinical Trial Manager who provides, in accordance with the appropriate quality standards, operational expertise and leadership to clinical operations teams to ensure the effective and efficient delivery of all operational aspects studies

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20.04.18 | Vollzeit | Schweiz | 100.000 - 125.000

Contacts equipment engineer when instruments are in need of maintenance/repair Manages material transfers with collaborating national and international research sites and external institutes Works closely with team members to provide effective solutions to support research and quality objectives and

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20.04.18 | Vollzeit | Schweiz | 100.000 - 125.000

Characteristics - Plans, monitors and manages internal design projects from initiation through completion - Ensures project results meet requirements regarding aesthetics, technical quality, reliability, schedule and cost - Monitors performance and recommends schedule changes, cost adjustments or resource

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20.04.18 | Vollzeit | Schweiz | 80.000 - 100.000

Replace the current Clinical Trial Directive (CTD) 2) The need to improve the efficiency and effectiveness of study start up and management and shorten the overall drug development timelines - MODS Standardization efforts support CTRi in meeting both those needs Objectives - MODS will develop data

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Top Job | Vollzeit | Schweiz

Manage all invoicing and validation aspects for a set of customers, products, suppliersAct as the main point of contact to research and resolve billing disputes and provide timely resolution on issuesImplement new measures to improve quality control process for outgoing invoicesPrepare monthly

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Top Job | Vollzeit | Schweiz

Qualification Expert Qualification Expert 1. Initiate, support and supervise equipment qualifications (including corresponding Major Accountabilities software qualification) in close collaboration with the analytical laboratories. 2. First point of contact to Quality Compliance in all topics

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