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Job Summary

Company
Beckman Coulter, Inc.
Location
Indianapolis, IN 46268
Industries
Biotechnology/Pharmaceuticals
Job Type
Full Time
Employee
Career Level
Experienced (Non-Manager)
Job Reference Code
BCI66855M

ADVANCED QUALITY INSPECTOR (2nd and 3rd shift)

About the Job

Beckman Coulter develops, manufactures and markets products that simplify,
automate and innovate complex biomedical testing. Our diagnostic systems are
found in hospitals and other critical care settings around the world and produce
information used by physicians to diagnose disease, make treatment decisions and
monitor patients. Instruments for life science research are used by scientists
as they study complex biological problems including the causes of disease,
identify new therapies, and test new drugs. Our customers include hospitals,
physicians' offices, diagnostic reference laboratories, pharmaceutical and
biotechnology companies, universities, medical schools and research
institutions. In fact, Beckman Coulter has more than 200,000 clinical and
research instrument systems operating in laboratories around the world.

The Advanced Quality Inspector inspects and reports on manufactured and supplied
parts quality. The incumbent will perform first article and in-process
inspections of injected molded plastic parts, record and monitor SPC data and
communicate adverse trends to engineering and production. They will train
production operators to do routine in-process inspections and monitor for proper
inspection techniques and data collection. They may also perform the inspection
of incoming materials, packaging and labeling components using more complex
inspection gauging. They have an understanding of basic Geometric Dimensioning
& Tolerancing systems. They also perform intricate First Article inspections
on a wide variety of parts. They initiate rejection reports for non-conforming
materials and ensure proper completion of required documentation in accordance
with departmental, GMP, and ISO requirements. They interface with Manufacturing
Engineering, Quality Assurance, Production, Planner/Buyers, Development
personnel, and suppliers when solving quality issues and troubleshooting parts.
The incumbent will create and analyze quality reports and recommend courses of
action regarding non-conforming materials.


QUALIFICATIONS
• 3-5 years of experience in a regulated (FDA, ISO, or GMP) manufacturing
setting
• Strong analytical skills
• Self starter
• Effective teamwork, interpersonal, and leadership skills
• Good written and verbal communication skills
• Experience with Microsoft Word and Excel
• Must be available to work any shift of a three shift operation


PREFERRED QUALIFICATIONS
• 2 year Associates degree in a technical field
• 2-3 years experience measuring parts using optical product gauging equipment
• Certified Quality Inspector
• Experience with material systems, such as, AMAPS or Oracle
• Knowledge of ISO13485 Medical Devices Standard

If you believe your education and experience are in line with the position
description and qualifications referred to above, and are motivated, energetic,
and looking for a new and exciting opportunity, please submit your resume online
at the URL below or at www.beckmancoulter.com .

AN EQUAL OPPORTUNITY EMPLOYER - We believe that the mutual goals of our business
and the community can best be met through our policy that consideration of race,
color, religion, ancestry, national origin, sex, age, disability, veteran status
or other protected characteristics, has no place in the selection, training or
promotion of employees. In furtherance of this policy, we have developed a
written Affirmative Action program to ensure positive action in providing equal

Apply Online : https://recruiter.kenexa.com/bci/cc/CCJobDetailAction.ss?command=CCViewDetail&ccid=bupJEdUjsTs%3D&job_REQUISITION_NUMBER=66855

 
 

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Beckman Coulter, Inc.