QMS & Quality Compliance Specialist (ISO-driven)

Maytav Bus Co; Garner (NC); On-site; USD 25,000 - 34,000; Full time

Job summary

Greene Resources in Garner, NC is seeking a Quality Compliance & Documentation Control Specialist to join a growing team. The role supports QA activities, maintains QMS documents, and assists in audits.

The position requires 2 years in quality control, ISO 9001/QMS knowledge, and proficiency in MS Office. Full-time, 7:00am–4:30pm, with a focus on cGMP compliance and continuous improvement.

Qualifications

• 2 years of experience in industrial quality control or related field.
• Experience with ISO 9001 Standards and Quality Management Systems (QMS).
• Advanced proficiency in MS Word, PowerPoint, and Excel (formulas, pivot tables).
• Understanding of calibration and traceability requirements.

Responsibilities

• Support QA Technicians with inspections, press/machine and comparator checks, and rework of defective products.
• Maintain accurate data, documentation, and controlled documents in the QMS, keeping them current and compliant with ISO, customer, and corporate requirements.
• Support internal and external audits and investigations, working with other departments to gather documentation.
• Develop and deliver document control and quality compliance training, and keep audit-ready training records.
• Analyze quality metrics (audits, nonconformances, complaints, training compliance, revision cycle times) in Excel to spot trends and produce clear, actionable reports.
• Lead cross-functional CPI efforts and drive CAPAs.
• Follow SOPs and current cGMPs.
• Other duties as assigned.

Skills

Quality control

ISO 9001

QMS

Analytical

Detail oriented

Communication

Education

High School diploma or GED

Internal auditor cert.

Tools

Excel

Word

PowerPoint

Job description

Greene Resources in Garner, NC is seeking a Quality Compliance & Documentation Control Specialist to join a growing team. The role supports QA activities, maintains QMS documents, and assists in audits.

The position requires 2 years in quality control, ISO 9001/QMS knowledge, and proficiency in MS Office. Full-time, 7:00am–4:30pm, with a focus on cGMP compliance and continuous improvement.