Design and develop new light emitting devices from III-V compound semiconductors materials.
Requires through knowledge and hands on experience with epitaxial growth on 3" and 4" GaAs or InP wafers
*** Conduct design of experiments
*** Set up, program, and operate thermal evaporation tools. (MOCVD, MBE)
*** Schedule runs, track process parameters
*** Implement lean manufacturing and six sigma initiatives
*** Develop manufacturing process instructions for epitaxy, photolithography ...
Utilize your knowledge of design, development, test engineering, and manufacturing processes involved with the creation of light based detection devices to develop and validate assemblies and housings for new and existing products.
*** Component lay out
*** Athermalization evaluation
*** Material selection and fabrication (Sheet metal, plastics, composites)
*** Finite element analysis and structural evaluation
*** Design using SolidWorks or similar 3D CAD software
Architecture firm in New City, NY is seeking an experienced Architect with 3-5 years experience in high end residential. Individuals must be able to design and produce construction documents, must have knowledge of zoning regulations, building codes, and deal with field issues with contractors. Position is for a full time, long term contract position for the right candidate..
Please provide resume, sample portfolio work and salary requirement.
Labor Ready is seeking qualified candidates for an Administrative/Data Entry position, in Chester, NY. Our customer is seeking a candidate with strong computer skills and customer service experience. This is a temp to hire position, : 1st candidate would work Sunday thru Tuesday 7 am to 7 pm and Wednesday 7 am to 1 pm. 2nd candidate would work Wednesday 1 pm to 7 pm and Thursday thru Saturday 7 am to 7 pm. It is a 42 hour work week. The pay ranges from $11.50- $12.50 per hour, based on experience.
Seeking at least 5 years directing and coordinating quality assurance activities for good clinical practices, coordinate and oversee inspections to ensure compliance to FDA regulations, IRB and IEC regulations and guidelines, site SOPs, protocols, and industry standards.
*** Direct and coordinate GCP quality assurance activities.
*** Author GCP documentation: protocols, case report forms, tables, listings, reports, and investigational brochures.
*** Plan and execute document audits and ...
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