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Contract Role || Quality Engineer || Warsaw, IN at Warsaw, Indiana, USA
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From:

Vijay Singh,

Quantum World Technologies Inc.

[email protected]

Reply to: [email protected]

Greetings,

Hope you are doing great today

I have an urgent requirement for Quality Engineer role based out Warsaw, IN.

Kindly go through the job description and let me know your interest. If you interested kindly share me your updated resume.

Here is the Position :

Role :

Quality Engineer

Location : Warsaw, IN

Experience Required : 2-4 years.

Job type : Contract

Top Skill Required :

Medical Devices, Process Validation, IQ/OQ/PQ, 21 CFR Part 11, Statistical Analysis Tools, Critical-to Quality (CTQ) Analysis, Inspection Techniques, SPC, Change Management System

Job Description :

Technical Skills :

knowledge of basic quality tools, risk analysis, statistics (SPC), and inspection techniques

Ability to read and understand engineering drawings

Specific experience with process characterization, equipment IQ/OQ, process OQ, and PQ

Specific experience with Test method Validation and Gage R&R

Experience with root cause analysis and problem-solving for both technical and process issues

Working knowledge of design control and cGMP requirements for medical device manufacturing per FDA QSR and ISO13485-2003

Good problem-solving skills through the use of quality and statistical tools

Ability to read and understand engineering drawings

Knowledge of basic quality tools, risk analysis (PFMEA), statistics (SPC), Critical-to Quality (CTQ) Analysis

Knowledge of Quality System requirements, ISO and FDA requirements

Experienced with control procedures, such as the Change Management System, Nonconformance Reports, Engineering Specifications, Corrective and Preventive Action (CAPA), and Work Instructions & Proficient with Statistical Process Control concepts, process development, CNC programming terminology, and tooling design concepts

Microsoft Office Suite and Project

Roles & Responsibilities :

Analyze/review the effectiveness of preventive and corrective actions. Review root cause investigation according to an established process.

Accountability and ownership of Quality metrics including maintenance and reviewing of leading and lagging indicators of quality

Develop, interpret, and implement appropriate process monitoring and control methods consistent with the level of process/product risk.

Collect data and execute/conduct various analytical/statistical analyses and interpretations as part of process improvements and day-to-day support.

Document, justify, review, or analyze whether a proposed change to a process will not enhance the risk level in some way beyond the capability of current controls or whether a change will result in potential non-compliance to a required standard such as the QSRs

Assess the need for risk mitigation techniques given product classification, potential defect types, defect frequency, severity, patient risk, process capability, process controls, etc. Determine the effectiveness of these techniques on previously implemented improvements

Interface with Manufacturing/Process Engineering, R&D, and Regulatory departments to resolve process issues and implement changes.

Apply knowledge of process control tools, statistical sampling, and other analytical techniques to maximize the quality and flow of products through the production line.

Identify, analyze, and manage risk through the product life cycle with the use of FMEA and other risk management tools.

Facilitate product and process Corrective and Preventive Action (CAPA) investigations from issue identification through the implementation of solution and effectiveness monitoring.

Execute equipment qualification or process validation project(s)

Thanks & Regards

Vijay Singh

Quantum World Technologies Inc.

www.quantumworldit.com

E-mail :
[email protected]

Office: +1-805-222-0532 ext: 244

linkedIn :
https://www.linkedin.com/in/vijay-singh-0b506022b/

Keywords: rlang golang
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06:41 PM 01-Sep-23


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Location: Warsaw, Indiana