As the Administrative Assistant of Neoteryx you will be the first point of contact and an essential representative for our company. The Administrative Assistant’s core duties and responsibilities are to ensure the front desk welcomes guests positively, and to execute all administrative tasks to the highest standards.
Your duties include providing administrative support throughout our organization. You host visitors, take charge of front-desk activities, redirect phone calls, distribute correspondence, organize activities, and have your finger on the company’s pulse.
To be successful as an Administrative Assistant, you should have a friendly and enthusiastic personality, particularly when performing customer-facing aspects of the role. You must have a penchant for streamlining and simplifying processes as you go, and should be able to handle emergencies quickly and effectively. Multitasking and stress management skills are key.
RESPONSIBILITIES/DUTIES
SUPERVISORY RESPONSIBILITIES
None
QUALIFICATIONS & PREFERRED EXPERIENCE
ABOUT NEOTERYX
Founded in 2014, Neoteryx is a medical device company shaping the future of healthcare. Our breakthrough blood collection technology – VAMS™ – is used by pharmaceutical giants, organ transplant patients, researchers in economically disadvantaged regions, and others on the leading edge of science and medicine. When you join our fun, tight-knit team, you’ll discover what one drop of blood can do, and be part of microsampling innovations that will change the world.
Contact Us
Trajan Scientific Americas Inc.
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Mitra® devices are intended as a specimen collector and for the storage and transport of blood. They are CE-IVD in the UK and EU, a Class 1 IVD in Australia, Brazil & China, Class B in South Africa, and registered with health agencies in Canada and Ukraine.
In the USA, Mitra devices are supplied as a Research-Use Only (RUO) product, to assist in method development, other research-related and non-diagnostic activities. Mitra has not been validated for use with any diagnostic testing. The suitability of Mitra for any analytical application must be evaluated and validated by the laboratory or research institute in a manner consistent with local regulatory requirements.
hemaPEN® is supplied for therapeutic or IVD use in Australia, New Zealand, UK, EU and USA only: ARTG number: 280007; CE mark, general IVD; US FDA number: D410490. Outside of the territories listed above, the hemaPEN is supplied for research use only (RUO) and not for therapeutic or diagnostic use.
Mitra®, VAMS® & hemaPEN® are registered trademarks owned by entities in the Trajan Group.
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