Product Support Specialist

CDI Corporation Mountain View , CA 94035

Posted 2 months ago

Job Order #395956 - G-REQ-00145774

Title: Product Support Specialist

Location: Mountain View, California

Please contact: April Mallari 404-609-4576 or april.mallari@cdicorp.com

Position Description

  • The Resource Management team is responsible for planning, procuring and managing machine and network resources.

  • The team has a broad expertise in infrastructure and data center technologies.

  • We build and use tools to monitor and manage hardware capacity.

  • We also manage hardware costs relating to IT budget.

  • Projects which the team manages include helping to prioritize among multiple feature launches, advising on resource optimizations and driving projects to improve efficiency.

  • The creation of dashboards is a big part of this role.

  • Being able to understand data and pull out relevant information to present recommendations for the team.

  • Those applying MUST have SQL experience and be able to data visualizations.

  • Our team supports operational work involved with day to day management of production data center machine resources.

  • We perform and track machine drains, monitor supply and take action for key thresholds.

  • We also allocate machine quota to services, and configure data center resource pools.

  • This role supports such internal customer requests.

Requirements:

  • BA/BS degree in computer science, mathematics, engineering, or equivalent experience.

  • 0-2+ years of work experience

  • Be proactive, strong analytical skills

  • Familiarity with excel/spreadsheets

  • Familiarity with google suite of applications: gmail, docs, sheets, and slides

Desired

  • 1+ years of work experience

  • Able to thrive and finish projects even when running into obstacles

  • Familiarity with IT environments Familiarity with customer request ticketing system or software Be an awesome person to work with

Prescreen Questions:

  • You are comfortable working around the core hours of 8 am to 5pm (Yes or No)?
  • List three times or examples (experiences) when you created a SQL dashboard *
  • Explain what a data center is in three sentences.

Technical Questions

  • Describe what a database is in three sentences. *
  • In SQL, what is a primary key? *
  • As best as you can, explain the importance of the term "data integrity"?
  • In SQL, list all of the different types of "Joins" that you know of. *
upload resume icon
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.
Mobile App Icon
Download the
LiveCareer app and find
your dream job anywhere
App Store Icon Google Play Icon
lc_ad

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
Regulatory Specialist Or Sr Regulatory Specialist New Product Development

Viewray

Posted 4 days ago

VIEW JOBS 1/19/2019 12:00:00 AM 2019-04-19T00:00 Job Summary This Regulatory Specialist will be focused on MRI and radiation therapy new product development projects. This individual will participate in project team meetings, guide the team on product and testing requirements and support FDA negotiations and submissions on behalf of the project team. Experience in the radiation space or similar medical devices is preferred in order to guide an active product development team. In addition, experience with FDA submissions and negotiations in the 510(k) space is required. This position will report to the Manager of Regulatory Affairs. Please submit your cover letter and resume to hr@viewray.com. For information on the company, please go to www.viewray.com. Responsibilities * Participate on New Product Development teams guided by a project manager to deliver regulatory deliverables * Be a business partner to drive efficient and positive team communications * Provide expertise to the product team on testing requirements and standards to follow to ensure minimal questions from regulatory agencies upon applications being submitted * Prepare global regulatory submissions, with the focus being on the U.S., Europe and Canada * Participate in the Regulatory function internally and partner with regulators to create a world class organization * Drive/participate in meetings with the FDA and Notified Body Education, Experience, Skills * AA or AS in biomedical, electrical/electronic, mechanical, or pure science discipline * 5+ years of successful experience in medical device Regulatory Affairs * Knowledge and experience with FDA Quality System regulations * Successful preparation and clearance of 510(k) applications with the FDA and Technical Files with a Notified Body * Experience in NRC regulated environment and knowledge of ISO and CE Mark requirements very preferable * Experience working with complex electro mechanical medical device systems utilizing complex software * Personal Interactions * Creative, flexible, and collaborative in approach to technical problem solving * Ability to communicate effectively, both orally and in writing, at a variety of technical levels * Ability to work effectively as part of the diverse team including physicists, scientists, and engineers in a fast-paced environment and with multiple projects * Please provide the name of any ViewRay employee referral for this position when you submit your cover letter & resume ViewRay provides equal employment opportunities to all qualified applicants without regard to race, sex, sexual orientation, gender identity, national origin, color, age, religion, protected veteran or disability status or genetic information. Viewray Mountain View CA

Product Support Specialist

CDI Corporation