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4 controls engineer ii jobs found

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Onsite controls engineer ii New York
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Full time  (4)
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QT
Mar 28, 2026
Full time
Controls Engineer II
QED Technologies Rochester, NY, USA
Summary Coordinates electrical and controls related engineering activities of outside suppliers to assure new product platforms achieve the desired functions, cost and schedule. Designs, builds and debugs systems of electrical, hydraulic, and pneumatic controls for CNC machines, related test equipment and facilities. Essential Duties and Responsibilities include the following. Other duties may be assigned. External Product Development Writes Controls requirements and specifications. Communicates requirements clearly and completely to suppliers. Develops validation plans to assure all controls requirements are properly implemented by supplier. Develops validation strategies to assure all motion control requirements are met by supplier. Work with suppliers or external consultants to verify machine design against electrical design standards as required to fulfill regional requirements. Typically, European CE requirements per Machinery Regulations, USA NEC code...
SW
Mar 13, 2026
Full time
Mechanical Engineer II
$80,000 - $100,000 yearly
Springs Window Fashions New York, NY, USA
Description Mecho is the leading commercial solar shading, and intelligent controls systems development manufacturer that has pioneered the industry and is committed to design and functional excellence. Our sales force is recognized for pioneering innovative and classic window management solutions to the Architecture, Design, and Engineering Community and supporting our network of Mecho Dealers. Our Department The Engineering department is at the heart of the Mecho brand. We are looked upon as the industry leader and must continue to strive to earn that place. We deliver innovative new products for the market as well as customized solutions for today's most challenging architectural designs. Our impact goes well beyond the window and must integrate our solutions into the building as a system and must positively impact the occupants as well as the building owners. Mission The main purpose of this role is to create, develop, testing, document and support innovative...
PP
Apr 02, 2026
Full time
Mechanical Engineer II
$76,900 - $115,400 yearly
Plug Power, Inc. Rochester, NY, USA
Mechanical Engineer II (Stack Engineering) Status: Exempt (Salaried) Department: Stack Engineering - 389 Location : Rochester, NY Position Summary In this exciting and creative role, you will be responsible for the design of custom fuel cell stack components and incorporation into higher level assemblies (both existing and new product configurations). Using engineering fundamentals, tools, and techniques, you will be responsible for the detailed design of various fuel cell components to meet cost, manufacturability, performance, and reliability requirements. The ideal candidate must be able to create and maintain large 3D CAD assembly models, individual part models/drawings, and associated bills of materials. As part of a cross functional team, you will plan out and conduct hands on prototype builds and testing to validate design functionality and feasibility for production release. The candidate should be creative, self-motivated, detail oriented, and able to handle...
CI
Dec 15, 2025
Full time
Research and Development Senior Medical Device Engineer
Cresilon, Inc. NY, USA
Cresilon ® is a Brooklyn-based biotechnology company that develops, manufactures, and markets hemostatic medical devices utilizing the company's proprietary hydrogel technology. The company's plant-based technology has revolutionized the current standard by stopping traumatic and surgical bleeds in seconds without the need for extended manual pressure. The company's current and future product lines target veterinary, human trauma, and human surgical applications. Cresilon's mission is to save lives. Learn more about the company at www.cresilon.com. Description: The Senior Medical Device Engineer is responsible for leading the design and development activities of new products and improving existing products in compliance with all quality and regulatory requirements. They will be responsible for authoring technical documents for the development of medical devices and combination products according to relevant Design Control regulations and standards. The person in this position...
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