This is a full time position (a minimum of 40 hours) based in Torrance, CA. This job requires no travel. The typical work schedule is Monday – Friday. The salary for this position is commensurate with experience and transferable skills and abilities. Manufacturing operations are located adjacent to the corporate office, so there is direct communication between sales, engineering, manufacturing, and shipping.
The Manufacturing Supervisor position is a key member of the Neoteryx team responsible for ensuring on time production of finished goods, prioritization of production, overseeing production and raw materials inventory, generation and updating of WKIs, facilitation of purchasing, shipping, and receiving functions and establishing a manufacturing environment that is focused on metrics and continuous improvement.
Neoteryx is a cutting-edge organization that researches, develops, manufactures, and sells medical devices, based on Volumetric Absorptive Microsampling (VAMS™) technology. Our mission is to deliver on the promise of microsampling technology, enabling biological specimen collection anytime, anywhere, by anyone, while reducing costs and improving the clinical experience.
Neoteryx LLC is committed to providing an environment of mutual respect. As such, Neoteryx is an Equal Opportunity Employer and does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need.
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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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