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Logistics specialist i

El Pueblito, Qro
Thermo Fisher Scientific
Publicada el 28 noviembre
Descripción

Work schedulestandard (mon-fri)environmental conditionsofficejob descriptionjob description: logistics specialist ilocation: chilethermo fisher scientific inc., a global leader in scientific research and development.thermo fisher scientific inc. is providing an outstanding opportunity for a supremely motivated logistics specialist i to become part of our top-tier team in chile. Being a part of the clinical trials logistics unit, you will fulfill a crucial role in ensuring the flawless delivery of clinical trial materials. Your determination and meticulous approach will play a pivotal role in upholding our high standards of quality and compliance.key responsibilities:arrange for the conveyance and dispersal of clinical trial supplies to multiple sites in chile.ensure all shipments align with regulatory requirements and company policies.monitor and track shipments to determine timely delivery and resolve any issues.maintain accurate records of all shipments and related documentation.collaborate with internal teams, including project managers, clinical operations, and quality assurance, to ensure seamless logistics support.communicate with external vendors and logistics providers to manage transportation and delivery schedules.assist in the preparation and review of shipping documentation, including customs declarations and import/export paperwork.support the development and implementation of logistics processes and procedures to improve efficiency and effectiveness.participate in regular team meetings and provide updates on shipment status and logistics activities.ensure compliance with all relevant health and safety regulations and guidelines.qualifications:bachelor's degree in logistics, supply chain management, business administration, or a similar field.at least 1-2 years of demonstrated expertise in logistics, supply chain, or a relevant sector, ideally within the clinical trials or pharmaceutical domain.demonstrates strong organization and time management capabilities, managing multiple tasks concurrently.strong communication and interpersonal abilities, capable of collaborating successfully with diverse teams and external collaborators.proficiency in microsoft office suite (word, excel, powerpoint) and logistics management software.diligent with a strong focus on accuracy and quality.capability to work autonomously and collaboratively within a dynamic work setting.familiarity with regulatory prerequisites and guidelines concerning the transportation of clinical trial materials is advantageous.proficiency in english and spanish is required.working conditions:the role may involve working outside of regular business hours to accommodate shipment schedules and urgent logistics needs.

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