Jobs

Quality Control Inspector

|  Posted On: May 11, 2026

location:Newark, DE 19702

Duration:6 Months, Contract

mode of work:On-site

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Job Summary

Job Title:  
Quality Control Inspector
Posted Date:  
May 11, 2026
Duration:  
6 Months, Contract
Shift(s):  

14:30 - 23:00

We care about you! Explore Rangam’s benefits information

Talk to our Recruiter

Name:
 
Meet Yadav

Email:
 
myadav@rangam.com

Phone:
 
650-516-3170

Description

Temp to Perm role

6 month assignment

Must be onsite - 100% onsite

2nd SHIFT: 2:30AM to 11:00PM

First 3-4 weeks will be on 1st shift 6:00 am - 2:30 pm for training

Job Summary

Performs inspections, testing, and sampling procedures for product manufacturing. Includes packaging line and incoming material checks. Reviews and releases Device History Records. May assist with validation or troubleshooting of testing methods.

  • Routine assignments with limited judgment
  • Acquires job skills and follows company procedures
  • Works under moderate supervision

Essential Duties and Responsibilities

  • Maintain and promote a safe work environment
  • Conduct inspections of in-process and finished goods
  • Record and maintain quality control documentation
  • Support investigations into non-conforming products
  • Support process audits for SOP and WI adherence
  • Initiate Non-Conforming Events (NCEs)
  • Review device history records and sales orders
  • Participate in Kaizen and continuous improvement initiatives
  • Complete training requirements and maintain records
  • Regular, punctual attendance and ability to work overtime

Physical Demands

  • Sit, stand, walk, reach, stoop, kneel, crouch, crawl
  • Lift/move up to 40 pounds
  • Exposure to mechanical parts, vibration, moderate noise
  • Safety shoes required in designated areas
  • May work with high voltage electronics, radiation, clean rooms, controlled environments, or dark rooms

Qualifications/Education

  • Minimum: High School Diploma or GED
  • Associate Degree preferred

Experience

  • 1-2 years preferred
  • Quality assurance or manufacturing experience beneficial
  • Experience in FDA-regulated medical device environment beneficial
  • Familiarity with Oracle ERP or Agile PLM beneficial

Skills

  • Basic Microsoft Office (Excel, Word, SharePoint, OneDrive)
  • Ability to follow written procedures
  • Effective written and verbal communication
  • Teamwork and independent work capability
  • High attention to detail
  • Ability to read schematics and blueprints
  • Familiarity with GMP and GDP

 

AI-Assisted Application Screening

As part of our recruitment process, we may use automated tools or AI-enabled technologies to assist with resume screening and candidate matching. These tools help our recruitment team review applications more efficiently, but they do not make hiring decisions. All final decisions are made by human reviewers.