Technical Logistics Specialist
Primary Location: Argentina, Remote ID de la oferta R0000041177 Categoría Clinical Logistics
sobre este trabajo
The Technical Logistics Specialist within CTS&L-LLS (Clinical Trial Supplies & Logistics – Laboratory Logistics Services) performs technical laboratory logistics tasks, in collaboration with other LLS personnel, ensuring that projects are progressing, and systems and documents are set up and maintained according to quality standards, Standard Operating Procedures and applicable ICH-GxP* and other applicable local regulation and industry guidelines.
Key Accountabilities:
Result Orientation and Project Execution
Contributes to the timely and efficient technical set-up of CTS&L systems at project level and to the development and completion of project specific documentation
Performs a variety of technical tasks during project conduct and closure phase of CTS&L projects
Contributes to IT system validation (testing, documentation)
Technical Acumen
Creates laboratory logistics print documents (forms, labels) based on provided specification
Communicates with print vendors to support timely print process and product delivery
Contributes to high-quality system setup within project context by creating and reviewing configuration documents, performing system setup and quality checks
Performs a variety of conduct tasks within the systems (e. g. laboratory data management, query resolution and trouble- shooting)
Supports creation of data transfer agreements, shipment list and reports specifications
Performs programming/validation tasks, e.g. for the generation of scripts (SAS, R, SQL or other) for data transfers, reports and shipment manifests
Participates in IT system validation processes
Skills:
Understanding of the regulatory framework of drug development and clinical laboratories
Good interpersonal, verbal, and written communication skills
Ability to work as team player in multi-disciplinary teams
Very good knowledge of Microsoft Office programs
Very good analytical skills
Self-motivated, professional attitude
A flexible attitude with respect to work assignments and new learning
Ability to execute multiple and varied tasks with enthusiasm and prioritize workload with attention to detail
Good English skills
Knowledge and Experience:
Previous employment or appropriate expertise in engineering/technology area preferred within the pharmaceutical industry
Good knowledge in databases and Windows operating system
Experience with programming (VB/VBA, SAS, R, Python or other) and/or desktop publishing tools is desirable
Data management/Lab data management work experience within CRO / pharmaceutical industry or laboratories is desirable
Demonstrated ability to work in teams.
Education:
Natural Sciences, Engineering, Informatics, Mathematics or Statistics degree
Vocational degree (i.e. Technical Assistant, Documentation Assistant or similar) and relevant working experience
Education as Graphic Designer or Technical Publisher
Previous employment or appropriate expertise in engineering/technology area preferred within the pharmaceutical industry.
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