Job Details

ID #6036358
Estado Delaware
Ciudad Newark
Tipo de trabajo Contract
Salario USD Depends on Experience Depends on Experience
Fuente Zenosys
Showed 2020-11-23
Fecha 2020-11-20
Fecha tope 2021-01-19
Categoría Etcétera
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Validation Engineer with Medical Device Testing - Skype Hire

Delaware, Newark, 19702 Newark USA

Vacancy caducado!

Hello, Zenosys is looking for Validation Engineer a client Newark, DE If you are available and interested in the below opportunity, please send me updated resume. Thanks

Onsite day1

Job Title Validation Engineer Location- Newark, DEDuration –12+ Months Contracts ( going to be Long Term )

If you are interested, please provide the following details along with the updated resume to

speed up the interview process. Full Legal Name as mentioned in Drivers' license:Current Location:Willing to relocate to the specified work location:Currently on a project or actively looking:Availability for interview:Availability to join the project:Date of Birth (Month/Date):Visa Status:Since how long the candidate has been in US:Highest Education Details along with Passing year: Main focus of this position is Validation and Verification. however as this group that i am working with

software driven electro-mechanical system which the candidate need to validate. therefore Siemens is looking for candidates with good software V&V (CSV-computer system Validation) as well as Hardware V&V (Equipment Validation) background. Please find some responsibilities below that I am performing.

Responsibilities:Ø Prepare validation and performance qualification protocols for new and/or modified processes, systems or equipment for healthcare industry.Ø Assist in the development, design/code, debug and implementation of electro-mechanical systems using LabVIEW architecture to test the clinical chemistry system and Immunoassay systems.Ø Ensure system compliance with Good Manufacturing Practice, Current Good Laboratory Practice, Current Good Documentation Practices, and FDA regulations such as 21 CFR Part 11, Part 210/211, Part 58, Part 810, and Part 820Ø Perform periodic review for computer systems, conduct GAP analysis and develop remediation plan.Ø Author technical documents (protocols, reports, standard operating procedures) to comply with regulatory requirementsØ Develop and establish effective Quality Control and associated Risk Management PlansØ Author/review and approve technical deliverables such as functional specification, verification plan, user requirement specification, functional requirement specification, design specification, test method validation, installation qualification protocol and summary report, operational qualification protocol and summary report, performance qualification protocol and summary report, test plan, test scripts which interact with Siemens proprietary Global Testing PlatformØ Review and test Diagnostics Communication Mechanisms with newly developed testersØ Provide technical support for very complex, highly critical programs and systems. Plan and coordinate tests, resolve production problems, identify opportunities to improve systems and architecture.Ø Maintain proficiency in programming languages, program development, testing and serve as an expert in area of responsibility.Ø Provide technical analysis and solutions to issues and technical direction.Ø Utilize technical expertise to manage multiple assignments, including large and critical projects to assure timely and cost-effect objectives delivery

If interested Please send me your resume at

Thanks,Hemendra Kalal, Ph: 732-967-4817(O) Fax: 732.584.2421Zenosys Consulting, Web: http://www.zenosys.com Disclaimer: If you have received this email in error or prefer not to receive such emails in the future, please reply with "REMOVE" in the subject line. All remove requests will be honored

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