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Quality Control Inspector

Location : Clifton NJ US 07013
Job Type : Temp/Contract
Reference Code : 21125-BZ1
Compensation : open - 20-22/h
Start Date : 08/01/2022
Hours : Full Time
Required Years of Experience : 2
Required Education : High School Diploma
Travel : No
Relocation : No
Job Industry : Engineering

Job Description :

  • Contract position for a Quality Control Inspector to perform testing and inspection activities for raw material and components.

  • Ensure that all SOP requirements have been met and if met, conduct the release activities.

  • Perform destructive and non-destructive testing on raw materials / components using Micrometers, Dial Calipers, Pin Gauges, Height Gauges, Thread Gauges, Optical Comparator, Micro Vu and other Precision Measuring Instruments.

  • Perform SAP Transactions and review both in-house and outside vendor processing/testing data for accuracy.

  • Provide guidance on lab and product related issues to Study Coordinators/SQE.

  • Attend MRB meetings when necessary.

  • Attend team meetings and provide feedback to team.

  • Gather data for engineering (PIR and MRB) investigations.

  • Make changes to existing SOPs.

  • Read, comprehend and follow job instructions and/or protocols direction including verbal, written, diagramed, colored, etc. and other work related documents.

  • Sort products by prioritization and schedule/delegate work to the QCRI inspectors.

  • Email, Data entry, prepare monthly reports, create change requests in PDM, trouble shooting and track product in SAP.

  • Provide judgement on product quality/acceptance and documentation.

  • Train technicians on various test methods, procedures and new policies.

Required Qualifications :

  • High School Diploma or equivalent is required:

  • Associates or BS degree in Science, Math, Business or related field preferred.

  • Member of American Society for Quality (ASQ), Certified Quality Technician (CQT) or Certified.

  • Minimum of 2 years in a quality function and working in a manufacturing environment is required.

  • Three to five years with quality experience in a FDA regulated environment is preferred.

  • Quality Auditor (CQA) is preferred.

  • Prior work experience with materials control and specialized testing is preferred.

  • Prior Training in CE Marking for EU Medical Devices Directives, FDA Quality Systems Regulations 21 CFR Part 820 ISO 13485 and Information Mapping is preferred.

  • Experience with SAP or equivalent system is required.

Contact: Bill Zukowsky

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