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QA Technician

  • QA Technician job type Posted on: Nov 01, 2026
  • QA Technician experience level Lancesoft INC
  • QA Technician employment type Mebane, North Carolina
  • QA Technician employment type Onsite
  • QA Technician salary Full-time

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Job Title :

QA Technician

Job Type :

Full-Time

Job Location :

Mebane North Carolina United States

Remote :

No

Jobcon Logo Job Description :

Job Description

Job Description

Job Title : Tech 1, Quality Assurance - Onsite

Location : Mebane, NC 27302

Contract Type : 3+ months on W2

Shift Timings : 1st Shift, Monday-Thursday, 7:00 AM - 5:30 PM

Payrate : $20.00 - $21.50/hour


Position Summary

We are seeking a detail-oriented Quality Assurance Technician I to support incoming quality inspection activities in a fast-paced FDA-regulated manufacturing environment. This role is responsible for inspecting incoming materials, components, and labels to ensure compliance with specifications, quality standards, and regulatory requirements. The ideal candidate will have experience in quality inspection, manufacturing, or quality control and possess strong attention to detail.

Key Responsibilities:

  • Perform incoming inspections of raw materials, components, and finished goods.
  • Conduct visual, dimensional, and functional inspections using calibrated measuring equipment.
  • Review inspection results against established specifications and sampling plans.
  • Identify, document, and segregate nonconforming materials.
  • Perform label inspections to ensure compliance with approved specifications.
  • Support product sampling, retention sample management, and device history record maintenance.
  • Maintain accurate inspection records in compliance with GMP and GDP requirements.
  • Assist with laboratory support activities, including sample collection and reagent preparation.
  • Participate in continuous improvement and Kaizen initiatives.
  • Follow all safety, gowning, PPE, and workplace procedures.

Required Qualifications:

  • High School Diploma or GED.
  • Minimum 2 years of manufacturing, quality control, or quality assurance experience.
  • Experience performing inspections and documenting results.
  • Strong attention to detail and organizational skills.
  • Proficiency with Microsoft Office applications.
  • Ability to work independently and in a team environment.

Preferred Qualifications:

  • Experience in FDA-regulated, medical device, pharmaceutical, or biotech manufacturing environments.
  • Knowledge of GMP (Good Manufacturing Practices) and GDP (Good Documentation Practices).
  • Experience using SAP or other ERP systems.
  • Familiarity with calibrated measurement equipment, sampling plans, and quality


Jobcon Logo Position Details

Posted:

Nov 01, 2026

Reference Number:

a837f7c2

Employment:

Full-time

City:

Mebane

Job Origin:

ziprecruiter

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Job Description

Job Description

Job Title : Tech 1, Quality Assurance - Onsite

Location : Mebane, NC 27302

Contract Type : 3+ months on W2

Shift Timings : 1st Shift, Monday-Thursday, 7:00 AM - 5:30 PM

Payrate : $20.00 - $21.50/hour


Position Summary

We are seeking a detail-oriented Quality Assurance Technician I to support incoming quality inspection activities in a fast-paced FDA-regulated manufacturing environment. This role is responsible for inspecting incoming materials, components, and labels to ensure compliance with specifications, quality standards, and regulatory requirements. The ideal candidate will have experience in quality inspection, manufacturing, or quality control and possess strong attention to detail.

Key Responsibilities:

  • Perform incoming inspections of raw materials, components, and finished goods.
  • Conduct visual, dimensional, and functional inspections using calibrated measuring equipment.
  • Review inspection results against established specifications and sampling plans.
  • Identify, document, and segregate nonconforming materials.
  • Perform label inspections to ensure compliance with approved specifications.
  • Support product sampling, retention sample management, and device history record maintenance.
  • Maintain accurate inspection records in compliance with GMP and GDP requirements.
  • Assist with laboratory support activities, including sample collection and reagent preparation.
  • Participate in continuous improvement and Kaizen initiatives.
  • Follow all safety, gowning, PPE, and workplace procedures.

Required Qualifications:

  • High School Diploma or GED.
  • Minimum 2 years of manufacturing, quality control, or quality assurance experience.
  • Experience performing inspections and documenting results.
  • Strong attention to detail and organizational skills.
  • Proficiency with Microsoft Office applications.
  • Ability to work independently and in a team environment.

Preferred Qualifications:

  • Experience in FDA-regulated, medical device, pharmaceutical, or biotech manufacturing environments.
  • Knowledge of GMP (Good Manufacturing Practices) and GDP (Good Documentation Practices).
  • Experience using SAP or other ERP systems.
  • Familiarity with calibrated measurement equipment, sampling plans, and quality


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