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Quality Engineer

Actalent Totowa, NJ

  • Expired: November 20, 2021. Applications are no longer accepted.


Coordinating the Validation Program including maintain the VMP, writing and executing protocol's , training other.

Participate or lead teams focused on customer requirement such as PPAP, Control plans, etc

Developed improved measuring methods to speed required inspection

Coordinate the implementation of using the CMM for Final dimensional inspection

Participate in continuous improvement projects

Communicate directly with customers to ensure their quality system needs are met

Supported root cause analysis for customer complaints and returns

Participate in customer and regulatory audits

Perform sterilization testing

Other projects and tasks as required by the Quality Manager



Quality Engineering

Quality Management system

Quality Assurance

ISO 13485

Medical device



Root Cause Analysis

Additional Skills & Qualifications:

Engineering degree



Root Cause Analysis

Quality Management System

Internal Audit


Quality Assurance

First Article inspection

ISO 13485

Medical Device

Experience Level:

Intermediate Level

About Actalent:

Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We’re supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.

The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.



Totowa, NJ



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