Quality Inspector 1

Jabil•Monument, CO

1d•Onsite

About The Position

At Jabil (NYSE: JBL), we are proud to be a trusted partner for the world's top brands, offering comprehensive engineering, supply chain, and manufacturing solutions. With 60 years of experience across industries and a vast network of over 100 sites worldwide, Jabil combines global reach with local expertise to deliver both scalable and customized solutions. Our commitment extends beyond business success as we strive to build sustainable processes that minimize environmental impact and foster vibrant and diverse communities around the globe. Summary/Objective The overall responsibilities of this position include inspection of in-house and vendor purchased products, and raw materials and services; inspection of packaging and labeling materials used for medical device. This also may include performing DHR review and “Release to Branch Plant” functions including document verification and recording incoming inspection inventory. Essential Functions (Reasonable accommodations may be made to enable individuals with disabilities to perform these essential functions.) Essential Functions required of all Inspectors are described below: Inspection Function: Inspects incoming, in process and finished products and material for visual, mechanical, and dimensional characteristics, using inspection sheets and applicable sampling plans. Prepares necessary documentation and insures paperwork compliance on all inspected items. Assist in the training of co-workers in new or improved techniques in areas of experience. Assists in identification and segregation of non-conforming materials / products. Works from inspection documentation, specifications, blue prints, written and verbal instruction. Performs “Roving Auditor” function involving inspection of product in a Manufacturing Flow Cell. Performs other related duties, as required. DHR Review Function: Performs Device History Review Inspection and final release of product to inventory control / warehouse. Performs filing and supports the imaging and verification process for Device History Records and other Quality System documentation. Other duties, as assigned. Know and follow all laws and policies that apply to one's job, and maintain the highest levels of professionalism, ethics and compliance at all times. Diligently participate in our compliance program-related activities as denoted by your supervisor. Communicate issues arising from daily builds and field reports that should be reviewed by a supervisor or engineer and being able to prioritize multiple tasks. Supervisory responsibilities This position does not have supervisory responsibilities.

Requirements

High school diploma or equivalent.
Ability to read and interpret measuring instruments, including but not limited to: calipers, micrometers, dial indicators, optical comparators, plug gauges, hardness testers, etc.
Proficient math skills, color verification and good hand/eye coordination.
Ability to communicate and work with various functional groups in a team environment.
Ability to learn PC applications required.
High level of concentration and attention to detail required ensuring products are properly labeled and packaged according to internal quality requirements.

Nice To Haves

ASQ (American Society for Quality) courses.
One year experience utilizing inspection techniques in Medical Device or Pharmaceutical Industry.
Experience with Microsoft PC applications.
Experience with MRP / ERP systems.

Responsibilities

Inspects incoming, in process and finished products and material for visual, mechanical, and dimensional characteristics, using inspection sheets and applicable sampling plans.
Prepares necessary documentation and insures paperwork compliance on all inspected items.
Assist in the training of co-workers in new or improved techniques in areas of experience.
Assists in identification and segregation of non-conforming materials / products.
Works from inspection documentation, specifications, blue prints, written and verbal instruction.
Performs “Roving Auditor” function involving inspection of product in a Manufacturing Flow Cell.
Performs Device History Review Inspection and final release of product to inventory control / warehouse.
Performs filing and supports the imaging and verification process for Device History Records and other Quality System documentation.
Know and follow all laws and policies that apply to one's job, and maintain the highest levels of professionalism, ethics and compliance at all times.
Diligently participate in our compliance program-related activities as denoted by your supervisor.
Communicate issues arising from daily builds and field reports that should be reviewed by a supervisor or engineer and being able to prioritize multiple tasks.