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1 Polarion Lifecycle Management (PLM) Manager Job in Moonachie, NJ

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Vantage MedTech
Moonachie, NJ | Full Time
$91k-113k (estimate)
4 Weeks Ago
Polarion Lifecycle Management (PLM) Manager
Vantage MedTech Moonachie, NJ
$91k-113k (estimate)
Full Time 4 Weeks Ago
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Vantage MedTech is Hiring a Polarion Lifecycle Management (PLM) Manager Near Moonachie, NJ

Polarion Lifecycle Management (PLM) Manager - Moonachie, NJ: Responsible for Quality Assurance to customize Polarion software to help clients during development of their medical devices. Develop processes, features, tools, and training to ensure Polarion software works properly. Document, analyze, create and test software or programs, including prototypes, based on and related to user or system design specifications and requirements. Work with fellow software and/or hardware team members in a cross-functional collaborate environment across all phases of the project lifecycle. Manage multi-person teams and work closely with customers, department heads and managers to improve processes, implement toolsets, and refine software training programs. Support the design and development of test software utilizing off-the-shelf commercial software test tools. Lead, mentor and develop a team to work on computer and information related projects. Analyze and audit processes and practices for inefficient or contradictory methods. Model identified business process problems to help generate efficient solutions. Implement, manage and evaluate operation processes and procedures, in accordance with the standards and procedures set out by the organization. Complete impact analyses for operations improvement by analyzing data form anomalies, trends and opportunities for improvement and participating in efforts to improve software capabilities.
Must have Master’s Degree in Biochemical or Chemical and Biochemical Engineering. Must have 2 years of work experience as Software Quality Assurance Engineer. Must have experience using Polarion ALM, GIT, Eclipse, and Fogbugs. Must have experience in medical device industry standards including Software Lifecycle, Quality Regulation Systems, Risk Management, and Class I, II and II Medical Devices. 40 hrs/wk, M-F, 9:00 a.m. - 5:00 p.m. Must have proof of legal authority to work in the United States. E-Mail your resume to

Job Summary

JOB TYPE

Full Time

SALARY

$91k-113k (estimate)

POST DATE

05/27/2024

EXPIRATION DATE

07/19/2024

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