Software Validation Engineer
Location : Clifton NJ US 07013
Job Type : Temp/Contract
Reference Code : 20817-BZ1
Compensation : open - 50-60/h
Start Date : 12/09/2021
Hours : Full Time
Required Years of Experience : 3
Required Education : AAS or BS Degree in Science, Math, Business
Travel : No
Relocation : No
Job Industry : Medical Devices
Job Description :
Contract position for a Software Validation Engineer for 12 months or longer for medical device manufacturing operations.
Work in project team to developing software user requirements, data migration plans, and functional requirements of new calibration management system.
Collaborate with calibration lab technicians to develop the user requirements of new calibration management system.
Develop software validation test cases.
Execute software validation protocols.
Generate change control notices for all computer software validation documents.
Create procedural revisions.
Responsible for calibration documentation assessment.
Work to project timeline and adhere to project deliverables.
Build Quality into all aspects of their work by maintaining compliance to all quality requirements.
Ensure compliance to all FDA and Worldwide Quality & Compliance regulations (As applicable to the job function).
Attend all required Quality & Compliance training at the specified interval.
Other duties as assigned.
Required Qualifications :
AAS or BS Degree in Science, Math, Business or related field is required.
Minimum 3 years with quality experience in a FDA regulated environment is preferred.
Experience in the medical device industry a plus.
Must have the education and experience to understand and comply with U.S. and Worldwide medical device regulations (As applicable to the job function).
Contact: Bill Zukowsky
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