Candidate must possess the ability to perform repetitive small assembly operations for extended periods of time. We will rely on this person to meet a daily part completion quota.
POSITION SUMMARY
The ideal candidate will have an eye for detail, and the ability to do repetitive small assembly operations. We will rely on this person to meet a daily part completion quota.
RESPONSIBILITIES/DUTIES
Responsibilities and Duties include but are not limited to:
PHYSICAL DEMANDS:
In general, the following physical demands are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to allow individuals to perform the essential functions of the job.
Assembly experience preferred but not required.
ABOUT NEOTERYXNeoteryx is a cutting-edge organization that researches, develops, manufactures, and sells medical devices, based on Volumetric Absorptive Microsampling (VAMS™) technology, to enable biological specimen collection anytime, anywhere, by anyone, while reducing costs and facilitating a patient-centric sampling experience.
This is a part time, temporary position that may lead to full time employment.
Title: Assembly Technician (Temporary Position)
Department: Production
Reports to: Manufacturing Manager
Supervises: n/a
Employee of: Neoteryx, LLC
Job Location: Torrance, CA (USA)
Job Type: Temporary
Salary: $13.00 /hour
Job Types: Part-time, Temporary
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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