Quality Inspector

Integrated Resources Inc.

Austin (TX)

On-site

USD 45,000 - 60,000

Full time

14 days+

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Job summary

A premier staffing firm is seeking a Quality Inspector to support corporate audits and ensure compliance during inspections. This role requires a minimum of 1 year of quality inspection experience, preferably in an FDA regulated environment. The ideal candidate will have excellent attention to detail, strong communication skills, and a background in interpreting technical instructions. Join an established company with a commitment to quality and service excellence.

Qualifications

Minimum 1 year experience in Quality Inspection or 2 years in a manufacturing environment.
Ability to interpret instructions and drawings.
Knowledge of ISO, FDA and QSR concepts preferred.

Responsibilities

Provide support for Quality System during audits and manage inspections.
Write and process Material Reject Reports.
Complete quality inspections following SOPs and product drawings.

Skills

Attention to Detail

Communication

Organizational Skills

Math Skills

Ability to Work Collaboratively

Education

High School or Trade School Graduate (or GED)

Tools

MS Office (Word, Excel, Access)

Job description

A Few Words About UsIntegrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty aretas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.

Job Description

Duration – 5 Months+ (Possible Extension)

· Provides support for the Quality System during corporate audits, actively participate in department activities and Perform audits of operations areas to confirm compliance with controlled procedures, as required

· Reviews and updates inspection plans as needed. Write DCO’s (Engineering Change Requests) to update as required. Assist Operations personnel in maintenance and updating of other Device Master Record documentation.

· Writes and processes Material Reject Reports, as necessary, and manage inventory that is on hold for quality inspection.

· Completes archival activities for device history records for lots inspected.

· Completes all required quality inspections following inspection instructions and/or product drawings. Use department databases to track and manage inspection workload and rejected products. Effectively follow SOPs, policies, and ISO/QSR requirements.

Experience:

· Minimum 1 year experience in Quality Inspection (or minimum 2 years in a manufacturing environment where responsible for measurement of products) and preferably in an FDA regulated environment.

· Ability to interpret instructions and drawings to effectively inspect product. Working knowledge of GD&T preferred.

· Ability to utilize multiple gauges and measurement tools for inspection of manufactured components and assemblies.

· Use of math skills relative to physical measurement of product (calculations involving basic functions and some geometry/trigonometry in English and metric units).

· Knowledge of ISO, FDA and QSR concepts and guidelines preferred.

· Excellent communication and organizational skills.

· Outstanding attention to detail.

· Ability to work with others in a positive and collaborative manner.

· Demonstrated ability to work accurately, follow instructions/schedules/timelines and handle multiple priorities.

· Knowledge of various MS Office applications such as: Word, Excel, and Access.

Qualifications

· Education: High School or Trade School Graduate (or GED) minimum.

· Certifications: Certified Quality Technician (ASQ CQT) would be a plus.

Additional Information

Thanks!!

With Regards,