Quality Engineer: ISO/AS9100 Audit & Process Improvement

Actalent; Tucson (AZ); On-site; USD 72,000 - 82,000; Full time

Benefits offered by this job

Medical, Dental, and Vision insurance

401(k) with company match

Generous PTO

Tuition Reimbursement

Paid Parental Leave

New Mother Benefits

Safety attire reimbursement

Job summary

Actalent in Tucson, AZ seeks a Quality Engineer to independently execute and improve QA processes across manufacturing and inspection, applying advanced tools and statistics to ensure QMS compliance and drive product quality and efficiency.

The role leads audits (ISO, AS9100), prepares documentation, closes findings, and conducts root cause investigations with CAPA using 5 Why and Fishbone methods. Permanent onsite position with a strong benefits package.

Qualifications

• Quality engineering
• Quality assurance
• PPAP
• Root cause analysis
• Supplier quality
• Audit
• AS9100
• Corrective action plans
• ISO 9001
• Inspection
• GD&T

Responsibilities

• Serve as a key quality representative for internal, customer, regulatory, and certification audits, ensuring compliance with ISO, AS9100, and other applicable standards.
• Coordinate audit preparation activities, maintain audit-ready documentation, facilitate auditor requests, and drive timely closure of findings and corrective actions.
• Lead root cause investigations and corrective action efforts arising from internal, customer, regulatory, and certification audits.
• Utilize methodologies such as 5 Why, Fishbone, and CAPA to identify systemic issues, implement sustainable solutions, and prevent recurrence.

Skills

Quality engineering

Quality assurance

PPAP

Root cause analysis

Supplier quality

Audit

AS9100

Corrective action plans

ISO 9001

Inspection

GD&T

Education

Experience requirement: 5 years with degree or 10 years without degree

Job description

Actalent in Tucson, AZ seeks a Quality Engineer to independently execute and improve QA processes across manufacturing and inspection, applying advanced tools and statistics to ensure QMS compliance and drive product quality and efficiency.

The role leads audits (ISO, AS9100), prepares documentation, closes findings, and conducts root cause investigations with CAPA using 5 Why and Fishbone methods. Permanent onsite position with a strong benefits package.