PPAP Quality Inspector & Documentation Specialist

Aptiv PLC; Warwick (RI); On-site; USD 52,000 - 68,000; Full time

Benefits offered by this job

Private health care

Life and accident insurance

Paid Time Off

Relocation assistance

Tuition Reimbursement

Job summary

Aptiv PLC in Warwick, RI is seeking a PPAP Quality Technician to support Production Part Approval Process documentation and inspections. You will collaborate with Quality, Engineering, Production, Purchasing, and Customer Service to meet customer requirements on time.

You’ll perform PPAP submissions, retain samples, and ensure compliance with ISO 9001 and IATF 16949 standards while maintaining precise records and communicating progress to management.

Qualifications

• Knowledge of PPAP submission processes and customer requirements.
• Ability to read engineering drawings and interpret specifications.
• Understanding of dimensional inspection methods and measurement techniques.
• Familiarity with PFMEA, Control Plans, MSA, SPC is a plus.

Responsibilities

• Prepare and compile PPAP packages per AIAG and customer requirements.
• Coordinate and track PPAP submissions through approval.
• Maintain PPAP records, approvals, and retained samples.
• Perform dimensional inspections on PPAP and production parts.
• Prepare dimensional reports and measurement documentation.
• Review material certifications and test reports for completeness.
• Support ISO 9001 and IATF 16949 compliance.
• Maintain a safe, clean work environment and participate in training.

Skills

PPAP requirements

Reading engineering drawings

Dimensional inspection methods

MSA / Gage R&R

SPC / Process capability

Cross-functional teamwork

Customer communication

Tools

Microsoft Excel

Microsoft Word

Microsoft Outlook

Job description

Aptiv PLC in Warwick, RI is seeking a PPAP Quality Technician to support Production Part Approval Process documentation and inspections. You will collaborate with Quality, Engineering, Production, Purchasing, and Customer Service to meet customer requirements on time.

You’ll perform PPAP submissions, retain samples, and ensure compliance with ISO 9001 and IATF 16949 standards while maintaining precise records and communicating progress to management.