Quality Assurance Associate - ISO 13485 (PPE)

NYES Protect; New York (NY); On-site; USD 50,000 - 65,000; Full time

Job summary

NYES Protect in Brooklyn, NY is seeking a Quality Assistant to support the Quality Department in daily inspection, documentation, labeling, and traceability across PPE manufacturing operations. The role focuses on maintaining accurate records and ensuring materials and finished goods comply with NYES procedures, regulatorystandards, and customer requirements under the ISO 13485 Quality Management System.

On-site, full-time position reporting to the Quality Manager/Director.

Qualifications

• High school diploma or equivalent required.
• Strong attention to detail and organizational skills.
• Basic familiarity with inspection, labeling, or document handling in a manufacturing environment is preferred.
• Willingness to be trained in ISO 13485 and AAMI PB70 quality and regulatory requirements.
• Comfortable working in a fast-paced production environment and learning structured quality procedures.

Responsibilities

• Assist with receiving inspections and basic sampling activities for raw materials and components.
• Perform visual inspections of seams, welds, labeling, and packaging during in-process and end-of-line quality checks.
• Support pallet verification and lot reconciliation to maintain product traceability before release.
• Ensure inspected and rejected materials are placed in their designated locations and document all findings in accordance with SOPs.
• Accurately complete inspection forms, checklists, and log sheets in both digital and physical formats.

Skills

Attention to detail

Organizational skills

Education

High school diploma or equivalent

Job description

NYES Protect in Brooklyn, NY is seeking a Quality Assistant to support the Quality Department in daily inspection, documentation, labeling, and traceability across PPE manufacturing operations. The role focuses on maintaining accurate records and ensuring materials and finished goods comply with NYES procedures, regulatorystandards, and customer requirements under the ISO 13485 Quality Management System.

On-site, full-time position reporting to the Quality Manager/Director.