Quality Control Inspector

Quality Control Inspector

Location: Newark, DE

Onsite Flexibility: Onsite

Contract Details

• Position Type: Contract
• Contract Duration: 7 months
• Start: June 15, 2026
• Pay Rate: $25.00 $31.00 / Hour (USD)
• Shift / Schedule: Monday Friday, 2nd Shift: 2:30 PM to 11:00 PM. Note: Initial training on 1st shift for approximately the first 3 4 weeks; 1st shift training hours are approximately 6:00 AM to 2:30 PM.
• Work Authorization: Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.

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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.

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Key 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
• Moving products from QC cells to packing cells

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Required Skills

• Attention to detail and quality mindset
• Adaptability ability to learn multiple SOPs and product lines; comfortable with cross-training
• Reliability consistent attendance and accountability (especially critical for second shift)
• Ability to follow written procedures and controlled documentation
• Effective written and verbal communication
• Teamwork and independent work capability
• Ability to read schematics and blueprints
• Familiarity with GMP and GDP
• Basic Microsoft Office (Excel, Word, SharePoint, OneDrive)
• Basic computer literacy (mandatory; system training provided)

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Preferred Skills

• One to two years of quality or manufacturing experience
• Medical device industry experience
• GDP and GMP experience
• Experience in other regulated industries such as aerospace, pharmaceutical, or automotive
• Familiarity with Oracle ERP or Agile PLM
• Quality assurance or manufacturing experience
• Experience in an FDA-regulated medical device environment

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Education Requirements

• Minimum: High School Diploma or GED (required)
• Associate Degree (preferred)

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Required Experience

• Prior manufacturing or quality experience appropriate for a Level II role
• Willingness and ability to work second shift

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Nice-to-Have Experience

• 1 2 years of quality or manufacturing experience preferred
• Quality inspection, final inspection, or Device History Record (DHR) exposure
• SOP-driven work history with evidence of documentation accuracy and audit readiness
• Experience in regulated environments (medical device, pharma, aerospace, automotive)

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Work Environment / Physical Requirements

• Work is 100% on site
• Sit, stand, walk, reach, stoop, kneel, crouch, crawl
• Lift/move up to 40 pounds
• Ability to push and move large systems on metal dollies; movement of systems from QC cell to packing cell is part of the role
• Exposure to mechanical parts, vibration, and moderate noise
• Safety shoes required in designated areas
• May work with high voltage electronics, radiation, clean rooms, controlled environments, or dark rooms
• Standard manufacturing and quality PPE as required on site

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Interview Process

• Initial phone interview followed by an on-site interview with the hiring team; two-round process preferred (30-minute phone screen, then on-site interview may include additional supervisor or group lead)

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Important Notes

• Early starts before June 15 are strongly encouraged if candidates are available sooner
• If a candidate starts after June 15, the assignment will be structured as a 6-month duration with the end date prorated based on the actual start date
• This role focuses on finished product inspection and final procedures before release it is NOT an incoming/raw material inspection role; minimal use of calipers or blueprint-based dimensional inspection
• Assignment length is six months from individual start date
• Potential for extension or conversion is not guaranteed

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Benefits

• Medical, Vision, and Dental Insurance Plans
• 401k Retirement Fund

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About the Client

Innovative medical technology firm focused on women's health.

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About GTT

GTT is a minority-owned staffing firm and a subsidiary of Chenega Corporation, a Native American-owned company in Alaska. We highly value diverse and inclusive workplaces and support Fortune 500 organizations across banking, financial services, technology, life sciences, biotech, utilities, and retail sectors throughout the U.S. and Canada.

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Job Number: 26-05196 Industry: Manufacturing & Operations

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