Quality Control Inspector - 2nd Shift

Martech Medical Products, Inc.

Harleysville (PA)

On-site

USD 42,000 - 60,000

Full time

2 days ago
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Benefits offered by this job

Medical insurance
Dental insurance
Vision insurance
FSA
401(k) plan

Job summary

Martech Medical Products is seeking a detail-oriented QC Inspector to support our medical device manufacturing operations. This role inspects components and finished products to ensure they meet quality standards and regulatory requirements.

The position operates on 2nd shift (4:00 PM – 2:00 AM) at our Harleysville facility. Requires high school diploma, 1–3 years of QC inspection experience, and proficiency with calipers, micrometers, and gauges.

Qualifications

  • High school diploma or equivalent.
  • 1–3 years of QC inspection experience in a manufacturing environment.
  • Experience using precision measuring equipment.
  • Strong attention to detail and documentation skills.
  • Basic math and English communication skills.

Responsibilities

  • Perform in-process and final inspections of parts and finished products.
  • Document inspection results and maintain quality records.
  • Use measuring tools such as calipers, micrometers, and gauges.
  • Review drawings, specifications, and work instructions.
  • Identify and report nonconforming materials.
  • Support production and engineering teams in resolving quality issues.
  • Ensure compliance with FDA, ISO 13485, GMP, and company requirements.

Skills

Attention to detail
Measuring equipment
QC inspection

Education

High school diploma

Tools

Calipers
Micrometers
Gauges

Job description

Quality Control (QC) Inspector – 2nd Shift
Martech Medical Products, Inc.

Harleysville, PA

2nd Shift: 4:00 PM – 2:00 AM

Full-Time | Onsite

Local Candidates Only!

Position Summary

Martech Medical Products is seeking a detail-oriented Quality Control (QC) Inspector to support our medical device manufacturing operations. This role is responsible for inspecting components and finished products to ensure they meet quality standards and regulatory requirements.

Key Responsibilities
  • Perform in-process and final inspections of parts and finished products.
  • Document inspection results and maintain quality records.
  • Use measuring tools such as calipers, micrometers, and gauges.
  • Review drawings, specifications, and work instructions.
  • Identify and report nonconforming materials.
  • Support production and engineering teams in resolving quality issues.
  • Ensure compliance with FDA, ISO 13485, GMP, and company requirements.
Qualifications
Required:
  • High school diploma or equivalent.
  • 1–3 years of QC inspection experience in a manufacturing environment.
  • Experience using precision measuring equipment.
  • Strong attention to detail and documentation skills.
  • Basic math and English communication skills.
Preferred:
  • Medical device, pharmaceutical, or regulated manufacturing experience.
  • Knowledge of FDA, ISO 13485, and GMP requirements.
  • Ability to read technical drawings and specifications.
Work Environment
  • Manufacturing and clean-room production environment.
  • Requires working with small, precision medical device components.
  • Use of microscopes, calipers, magnifiers, and other inspection equipment.
  • Must follow all safety, quality, and GMP requirements.
  • Fast-paced team environment focused on quality and continuous improvement.
Physical Requirements
  • Ability to sit or stand for extended periods.
  • Manual dexterity for handling small components.
  • Ability to lift up to 25 lbs.
  • Excellent close vision and attention to detail.
Why Join Us?
  • Competitive pay
  • Medical, dental, and vision insurance
  • FSA
  • 401(k) plan
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