Easter Seals Jobs

Top 3-5 skills, experience or education required for this position:

• The engineer will have a technical leadership role for designing and testing FPGA functions

• He or she develops a thorough understanding of design requirements to ensure that the system’s objectives are properly defined and ultimately achieved

Qualifications

• BS in Electrical Engineering, Software Engineering or equivalent degree

• Must have at least eight years of FPGA design and development experience; prefer ten years of experience

• Prefer at least three years of experience in medical devices, ideally class II devices

• Individual will complete work with minimal supervision of the manager

• Ability to set medium term project goals and outline schedules for multiple tasks for several team members

• Strong team player with the demonstrated abilities and willingness to wear “multiple hats” and perform a wide range of tasks within a dynamic environment

• Individual must have strong verbal and written communication skills

• Responsible for performing all duties in compliance with FDA’s Quality System Regulation (QSR), ISO13485 , the Canadian Medical Device Regulations, and all other international regulatory requirements with which ZELTIQ complies

Responsibilities

• The FPGA Engineer will work collaboratively with a team to d esign and develop medical products from initial concept through the transfer to production

• The engineer will have a technical leadership role for designing and testing FPGA functions

• He or she develops a thorough understanding of design requirements to ensure that the system’s objectives are properly defined and ultimately achieved

Essential Duties and Responsibilities include the following (other duties may be assigned.):

• Act as a technical lead for product development projects

• Provide mentoring and guidance to other team members

• Outline and execute to short-term goals to achieve overall project milestones

• Prepare, present, and document designs at technical reviews

• Refine and develop selected concept(s) with little guidance from manager

• Plan, perform, and document verification testing

• Coordinate testing by other team members,

• Help develop assembly procedures and assist in transfer methods to manufacturing

• Document ECO changes within the Document Control system

• Coordinate design tasks for other team members for complex product designs

• Coordinate design constraints within R&D groups

• Resolve any design conflicts with preferably no managerial intervention

• Will typically be the technical leader

• Proficient with basic standard concepts and constraints involved in creating new product designs

Job Description

• The FPGA Engineer will work collaboratively with a team to design and develop medical products from initial concept through the transfer to production.

• The engineer will have a technical leadership role for designing and testing FPGA of the overall system product.

• Skills in FPGA are required. He or she develops a thorough understanding of design requirements to ensure that the system’s objectives are properly defined and ultimately achieved.

Essential Duties and Responsibilities include the following (other duties may be assigned.):

• Familiar with Xilinx tools: Vivado and Vitis

• Familiar with: Artix7 (or similar not to box in too much)

• Familiar with: MicroblCliente embedded core, and C programs

• Familiar with troubleshooting

• Familiar with FPGA HLS and combining with C

• Hands on with FPGA

• Familiar with porting FPGA to FPGA

• Familiar with port FPGA to microcontrollers

• Familiar with ST Micro

• Familiar with Python

• Familiar with Xilinx build processes

• Act as a technical lead for product development projects. Provide mentoring and guidance to other team members.

• Outline and execute to short-term goals to achieve overall project milestones

• Prepare, present, and document designs at technical reviews.

Qualifications and Additional Requirements:

• Responsible for performing all duties in compliance with FDA’s Quality System Regulation (QSR), ISO13485, the Canadian Medical Device Regulations, and all other international regulatory requirements with which ZELTIQ complies.

About US Tech Solutions:

US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit www.ustechsolutions.com.

US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.