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Validation Engineer -Medical Device & Regulations at Remote, Remote, USA
Email: [email protected]
http://bit.ly/4ey8w48
https://jobs.nvoids.com/job_details.jsp?id=2255733&uid=

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aJAY,

KK Software Associates

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Job Role :- Validation Engineer -Medical Device & Regulations
Work Location:- TCS - Minneapolis Downtown, MN -Plymouth, MN - Onsite

Role Description:
Competencies: EIS : Medical Device & Regulations
Experience (Years): 4-6
Essential Skills:
Must be proficient in wet chemical methods including measuring, mixing, pipetting, and weighing chemicals, as well as interpreting lab results
Microbiological and analytical laboratory tests in the medical or pharma industry preferred
Experience working with liquids, solutions, and reagents.
Experience in GLP, GDP, and laboratory investigations
Utilize standard laboratory equipment
The incumbent will follow good practices in recording and reporting data; and have a working understanding of FDA regulations, international standards, and guidance documents applicable to medical devices.
Experience with computer record-keeping systems is required
Experience with scientific and technical data processing and graphing software is required.
Excellent Interpersonal / communication skills, Organizational / planning and Project management skills preferred
Personal computer skills, Windows: word processing, presentation, e-mail, web browsers & spreadsheet software
Ability to work efficiently, meet timelines, and communicate status (generate trackers, send emails, etc.)

Keywords: Bacterial endotoxin (LAL) testing, Total Organic Carbon (TOC), protein and carbohydrate quantitation, water quality monitoring, Engineering and electrical testing, Installation Qualification, Operational Qualification, Performance Qualification, Validation

Keywords: Minnesota
Validation Engineer -Medical Device & Regulations
[email protected]
http://bit.ly/4ey8w48
https://jobs.nvoids.com/job_details.jsp?id=2255733&uid=
[email protected]
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02:24 AM 14-Mar-25


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