Quality Control Inspector - 2nd Shift
Martech Medical Products
Harleysville, PA
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JOB DETAILS
JOB TYPE
Full-time
SKILLS
Biotech and Pharmaceutical, Cleanroom, Communication Skills, Dental Insurance, Detail Oriented, Documentation, English Language, FDA (Food and Drug Administration), GMP (Good Manufacturing Practices), High School Diploma, ISO (International Organization for Standardization), Lift/Move 25 Pounds, Maintain Compliance, Manual Dexterity, Manufacturing, Manufacturing Operations, Mathematics, Medical Equipment, Medical Office Administration, Medical Products, Physical Demands, Problem Solving Skills, Production Support, Production Systems, Quality Control, Quality Management, Quality Metrics, Record Keeping, Regulatory Requirements, Technical Drawing, Vision Plan
LOCATION
Harleysville, PA
POSTED
Today
Quality Control (QC) Inspector – 2nd Shift
Martech Medical Products, Inc.
Harleysville, PA
2nd Shift: 4:00 PM – 2:00 AM
Full-Time | Onsite
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.
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.
- Medical device, pharmaceutical, or regulated manufacturing experience.
- Knowledge of FDA, ISO 13485, and GMP requirements.
- Ability to read technical drawings and specifications.
- 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.
- 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.
- Competitive pay
- Medical, dental, and vision insurance
- FSA
- 401(k) plan
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