Quality Inspector - Saint Paul, Minnesota | CareerCircle
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Quality Inspector

Actalent

02/21/2022

Posting ID: JP-002658987

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Saint Paul, Minnesota
Full Time
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Description:

- Reviews technical paperwork for accuracy and completeness. - Proactively works with documentation owners to remedy errors and omissions in quality records. - Provides the Design Assurance group with technical support as required. - Perform final manufacturing Device History Record (DHR) review at close of manufacturing process and product release. - Sets up and runs experiments and/or tests apparatus with direction. - Works with measurement tools including calipers, micrometers, pin gauges, and CMMs to ensure parts conform to specifications. - Provides input in evaluation of equipment and processes. - Troubleshoots = May repair, modify, and/or maintain systems and/or equipment. - Identifies and evaluates procedures to ensure the production of quality product for development organization. - May write technical reports, records of standards and rejections and other required quality documentation. - Demonstrates safe work habits, maintains clean and safe work area. - Willingness to provide and receive constructive input and feedback.

Skills:

first article inspection, documentation review, test documentation, quality control, micrometer, gages, calipers, inspection equipment, inspection of parts, inspection report, inspection gauges, quality assurance testing, quality standards, quality inspection, quality management system

Top Skills Details:

first article inspection,documentation review,test documentation,quality control

Additional Skills & Qualifications:

- 1+ years experience of medical device inspection experience whether it be receiving, in process, or final inspection - Two-year technical degree - Must understand clean room procedures and be comfortable working within one - Must have 1+ year of experience working from blue prints, using micrometers, calipers and other inspection tools - Knowledge of Quality Systems, FDA regulations, ISO 13485, and applicable worldwide regulatory requirements. - Working knowledge of IMTE and can understand/implement good documentation practices (GDP). - Ability to read technical drawings and follow inspection plans.

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.

Contact Information

Recruiter: Jean Chambers

Phone: (410) 579-3072

Email: jchambers@careercircle.com

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