Sorry, this job is no longer accepting applications. See below for more jobs that match what you’re looking for!

Senior Software Engineer (C/C++/Linux)

Expired Job

Cybercoders Acton , MA 01720

Posted 2 months ago

Minimum Required Skills:
C/C++, Linux, Linux Device Drivers, PCIe, Ports, Sockets, High Speed, Python, Bash, RTOS

If you are a Senior Software Engineer with C/C++ and Linux experience, please read on!

We are headquartered in the beautiful Acton, MA area and we are a cutting edge electronics manufacturer that partners with some of the countries largest players in the medical and security spaces. We employ old-fashioned engineering with our cutting-edge technology to separate ourselves from the pack. We have a smaller, fast paced team that loves staying up to date with the latest/greatest technologies.

We need a skilled Senior Software Engineer who is well versed with C/C++ and Linux Device Drivers. This person will work with software close to hardware, and high-speed data acquisition to work on projects in medical imaging, security imaging, and industrial imaging. Our products all involve acquiring data at rates up to and exceeding 2.5Gb/sec over commercial and custom PCIe interfaces and over network interfaces, and this person will be entirely or partially responsible for the system control software for imaging capital equipment.

Top Reasons to Work with Us

  • Outstanding work environment

  • Work with cutting edge technology

  • Significant room for growth

What You Will Be Doing

  • Help lead the system control software for imaging capital equipment

  • Work heavily with C/C++ and Linux Device Drivers

  • Participate in the development of specification, architecture, interfaces, software test design, implementation and automation

  • Work on projects in medical imaging, security imaging, and industrial imaging

What You Need for this Position

More Than 5 Years of experience and knowledge of:

  • C/C++

  • Linux Device Drivers

  • PCIe Drivers

  • High Speed Data processing

Strong nice to haves:

  • Python

  • Port and Socket Communications

  • Bash

  • RTOS

What's In It for You

  • Vacation/PTO

  • Medical

  • Dental

  • Vision

  • 401kSo, if you are a Senior Software Engineer with C/C++ and Linux experience, please apply today!

Applicants must be authorized to work in the U.S.Please apply directly to by clicking 'Click Here to Apply' with your Word resume!

Looking forward to receiving your resume and going over the position in more detail with you.

  • Not a fit for this position? Click the link at the bottom of this email to search all of our open positions.

Looking forward to receiving your resume!


CyberCoders, Inc is proud to be an Equal Opportunity Employer

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status, or any other characteristic protected by law.

Your Right to Work

  • In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification document form upon hire.

Copyright 1999 - 2018 . CyberCoders, Inc. All rights reserved.

C/C++, Linux, Linux Device Drivers, PCIe, Ports, Sockets, High Speed, Python, Bash, RTOS - C/C++, Linux, Linux Device Drivers, PCIe, Ports, Sockets, High Speed, Python, Bash, RTOS
Full-time, Employee

See if you are a match!

See how well your resume matches up to this job - upload your resume now.

Find your dream job anywhere
with the LiveCareer app.
Download the
LiveCareer app and find
your dream job anywhere

Boost your job search productivity with our
free Chrome Extension!

lc_apply_tool GET EXTENSION

Similar Jobs

Want to see jobs matched to your resume? Upload One Now! Remove
Manufacturing Quality Engineer

Insulet Corporation

Posted 1 week ago

VIEW JOBS 11/3/2018 12:00:00 AM 2019-02-01T00:00 Position Summary The Sr. Manufacturing Quality Engineer will be a critical contributor in a mission that truly represents an once-in-a-lifetime opportunity to join a company that is making significant investments in establishing US manufacturing, expanding internationally, and delivering a consistent cadence of product innovations to the market and investing in its people. The successful candidate will be responsible for providing Quality Engineering support to manufacturing helping to ensure delivery of highest quality product to the customer. It requires creativity and foresight to work with other functions to ensure compliance and the accomplishment of departmental and company goals. The position requires working alongside with engineering, purchasing, suppliers, and manufacturing to support the manufacturing operations and continuous improvement initiatives. Responsibilities * Assist in designing, building, and managing the facility Quality System to achieve compliance with ISO13485, ISO14971, 21 CFR part 820 and 11.• Performs and documents Root Cause investigations related to product and components rejections. Formulate corrective and preventive actions; implements those actions in order to improve quality levels and regulatory compliance.• Act as a backup Quality Manager as needed• Provide validation support by applying manufacturing quality tools including, but not limited to: FMEA, DFMEA, PFMEA, IQ, OQ, PQ, control plans, process verification/validation plans, Cpk, Cp, SPC, DOE, process data analysis, and DMAIC.• Write and review protocols and reports of Process and Test Method Validations. Design, complete protocols and write reports for gauge R&R analysis.• Write and review quality documentation such as procedures, test protocols and reports.• Prepare reports by collecting, analyzing, and summarizing data. Analyze data and make decisions using valid statistical techniques.• Assist in the creation of statistical techniques for metric generation methods.• Assist in the development of risk based assessments to determine inspection requirements and acceptance criteria.• Establish statistical confidence by identifying sample size and acceptable error; determine levels of confidence.• Support operations/manufacturing by resolving process and material related quality problems in support of the various manufacturing departments.• Work with operations/manufacturing and the contract manufacturer to lead efforts to resolve issues that involve quality system gaps, production non-conformances or situations that involve component qualification or procurement.• Work with department leads in identifying and establishing quality related metrics.• Assist in the development of process monitoring and measurement tools.• Establish ownership responsibilities for issues and non-conformances and develop expertise in Master Control to coordinate resolution of the issues and non-conformances.• Generate and maintain Quality System documentations (SOPs, procedures, forms, work instructions, etc.)• Enhance quality system processes as it pertains to management of assigned deliverables to ensure compliance.• Supervise Quality Technicians.• Train plant employees on new processes and programs (SPC, visual aids, new procedures, best practices, etc.)• Expected to be able to manage critical projects with little or no direction from QA manager.• Support plant cost reduction and process improvement projects through the use of various quality tools such as FMEA, process capability, Gauge R&R, Chart analysis etc.• Apply SPC methods for analyzing data to evaluate the current process and process changes• Be an active lead auditor, participating in external supplier audits and internal audits. • Develop and/or manage some quality programs related to resolution of issues arising from manufacturing operations as well as post manufacturing activities. Provide QA Engineering support and expertise to Manufacturing, Engineering, and other company functions.• Work with and guide the team performing incoming inspection, in-process control and final product testing and release to ensure deliverables of product release are met.• Support activities as it pertains to sterilization release, sterilization validation, biocompatibility, design verification, design validation and other associated validation and qualification activities.• Track and prepare reports related to Quality Metrics and identify and implement improvements towards meeting those goals.• Presents quality data to Management• Actively work within the CAPA system, provide inputs to the CAPA Review Board and Monthly Data Analysis.• Perform other duties as assigned. Education and Experience Minimum Requirements:• BS degree in engineering, a technical or scientific discipline. Preferred Skills and Competencies: • Minimum of 3 years in the Medical Device Industry, specifically in a Quality function working with QSR and ISO 13485.• Experience with FDA and ISO 13485 inspections.• Demonstrated experience/results in Quality System tools and problem solving.• Six Sigma and Lean Certification.• Effective verbal and excellent technical writing skills.• Ability to communicate and work effectively at multiple levels within the organization.• Must be able to multitask and prioritize autonomously• Ability to organize and judge priorities.• Excels at generating and maintaining organized and accurate records.• PC skill, word processing, spreadsheet, database.• High-mechanical aptitude and knowledge of device manufacturing methods are strongly preferred.• Knowledge of applied statistics (sampling plans, Cpk, population comparison, confidence analysis etc.) required.• Proficient in Statistical Software for data analysis (Minitab preferred) Physical Requirements (if applicable): * While performing the duties of this job, the employee is regularly required to sit, stand, and walk.• Employee must occasionally lift and/or move up to 50 pounds.• Able to travel internationally (10%) Insulet Corporation Acton MA

Senior Software Engineer (C/C++/Linux)

Expired Job