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For your reference, we have included the original job posting below.




Quality Control Laboratory Technician Job


Job Number:25138094
Company Name:Becton Dickinson
Job Location:Burlington, NC US
Job Category:Manufacturing & Production
 

Quality Control Laboratory Technician Job
Quality Control Laboratory Technician-QUA100FJ

BD, a leading global medical technology company that makes and sells medical devices, instrumented systems and reagents, is dedicated to improving people's health throughout the world. BD is focused on improving drug therapy, enhancing the quality and speed of diagnosing infectious diseases, and advancing research and discovery of new drugs and vaccines. The Company's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, BD employs more than 25,000 people in approximately 50 countries throughout the world.

BD Diagnostics Women's Health and Cancer develops, manufactures, markets, and sells innovative solutions to improve the clinical management of cancer, including detection, diagnosis, staging, and treatment.

BD is an Equal Opportunity/Affirmative Action Employer.

About us

Description

Basic Job Purpose:

Execute analytical and functional quality control test methods using standard lab equipment (e.g. spectrophotometer, GC, electrophoresis equipment, pH meter, etc.) to evaluate quality of reagents manufactured to defined specifications. Assist or perform other Quality Control (QC) department functions such as stability testing, testing of product returns or retains, validation studies, management of retained samples and instrument and equipment maintenance as directed.

Principal Accountabilities:

* Inspect incoming, in-process and finished goods for compliance with established quality specifications. Work with manufacturing, receiving and materials personnel to complete required QC testing, documentation and status labeling in a timely manner. Update material status in inventory system as necessary.
* Perform laboratory testing such as analytical testing (e.g. pH, densitometer, spectrophotometer, GC), immunoassays (western blot, ELISA) and cytological/histological testing (PrepStain, immunocytochemistry). Report and summarize results.
* Analyze data to specifications and designate as accept/reject. Initiate documentation for nonconforming materials as required.
* Assist with management of retention materials, equipment maintenance and other projects as directed.
* Work with Manufacturing Technologies and New Product Development teams to inspect and test first article components and participate in validation studies.
* Assist with development of new and revised quality control specifications and methods.
* Execute post market stability program including writing protocols and reports and analyzing data and presenting results.
* Assist with testing of product returns and performing investigation of product complaints.
* Perform bioburden testing to defined procedures for monitoring of high purity water system.
* Ensure that equipment is cleaned and maintained according to work instructions.
* Assist with cross-training and mentoring other technicians.
* Participate in continuous improvement activities (e.g. kaizen).
* Prepare, analyze, and distribute quality metrics (including SPC charts). Recommend action plans for unfavorable trends.
* May participate on extended core teams as a QA/QC representative.
* Handle hazardous waste as appropriate.
* Maintain 5S of work area.
* Additional responsibilities as assigned by QA management.

Job Dimensions:

* Operation of automated staining systems and other laboratory equipment
* Good communication (written and oral) skills and the ability to work in a multidisciplinary team environment are essential
* May act as team leader in the absence of area supervisor
* Must be able to work with hazardous chemicals in a safe manner
* Position requires occasional overtime as designated by Operations/Quality management. Overtime duties may be outside of direct area of responsibility.
* This position requires that the employee be present at designated shift start up times to ensure smooth production operation. Schedule may need to flex based on business needs. Position may require nontraditional work weeks such as 4/10 hour days.

Qualifications

Education and Experience Required:

* High school diploma/GED with a minimum of 3 years related laboratory experience
* Experience with sampling techniques, inspection standards, use of dimensional measuring tools, or use of analytical laboratory equipment (e.g. spectrophotometer, GC, pH meter)
* Knowledge of basic chemistry
* Excellent basic math skills and the ability to utilize Excel for basic calculations and graphing
* Must be able to speak, read, and write English fluently as well as write technically and summarize information into data reports
* Ability to lift at least 25 lbs unassisted
* Good attention to detail and the ability to work independently as well as in team situations
* Capability of prioritizing responsibilities and completing tasks on schedule

Education and Experience Preferred:

* Associate's degree or higher in quality or science related field
* Knowledge of immunoassay testing
* Experience using automated staining or imaging platforms
* Knowledge of Lean Manufacturing/Continuous Improvement
* Experience in histology or cytology slide preparation and imaging
* Knowledge of basic validation requirements or experience in performing method validations
* Knowledge of statistical techniques including use of data analysis programs such as Excel or Minitab and application of sampling plans
* Ability to design spreadsheets for QC applications
* Knowledge of SPC charts/development of metrics

Supervisory Responsibility:

* None

Job
Quality Control

Primary Location
US-North Carolina-Burlington

Shift
First Shift / Day Job

Relocation Available
No


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