At PacSci EMC, When Milliseconds Matter™, quality is not a department — it is a discipline embedded in every product we build.
We are seeking a Quality Specialist to execute and help mature a proactive product surveillance program across our manufacturing cells. This is a highly visible, floor-embedded role designed to reduce scrap, prevent escapes, and strengthen quality performance through real-time engagement in the build process.
This is not a desk-based QMS or Quality Engineer position. This role will serve as a roving quality presence across manufacturing operations, independently conducting product and process surveillance, supporting inspection and first article activities, and exercising stop-work authority when a nonconformance is identified. Success requires the judgment and communication skills to turn quality concerns into constructive coaching moments while maintaining strong partnerships with Operations.
Key Responsibilities
Product Surveillance & Audit Execution (Primary Focus – ~60–70%)
• Execute proactive product surveillance audits across aerospace manufacturing programs.
• Observe product builds in real time to verify adherence to inspection criteria, work instructions, documentation, and process requirements.
• Exercise authority to stop or pause production when a nonconformance is identified, then engage cell leadership and the appropriate quality or engineering resources to address the issue.
• Conduct approximately 30 surveillance audits per week across prioritized programs as a core performance expectation.
• Support AS9102 First Article Inspection (FAI) and workbook/documentation closeout activities, including review of parts inspection information and build records.
Process Audits & Manufacturing Discipline (~30–40%)
• Conduct process audits including PPE compliance, hazardous material controls, work instruction adherence, and calibration status.
• Verify that manufacturing documentation and traceability requirements are consistently met.
• Collaborate with Manufacturing Quality Engineers (MQEs) and Operations to identify systemic audit themes and determine appropriate follow-up actions.
Root Cause & Corrective Action
• Participate in and support structured root cause analysis and corrective action activities using methods such as 5-Why, Fishbone, and 8D.
• Partner with MQEs and cross-functional teams to help implement and sustain corrective actions that prevent recurrence.
• Support reduction of scrap, rework, PRB involvement, and cost of poor quality (COPQ).
• Maintain and track corrective action progress as required.
Data Analysis & Continuous Improvement
• Collect and analyze quality data to identify trends, high-risk build activities, and areas where product surveillance should be prioritized.
• Use Excel, Pareto charts, Power BI, and other available analytical tools to communicate trends and prioritize improvement efforts.
• Support measurable reductions in defect rates, scrap, rework, and operational waste through proactive surveillance and follow-up.
• Contribute to lean and continuous improvement initiatives within manufacturing cells.
APQP & Quality Systems Development
• Support the execution and maturation of APQP-related tools (PFMEA, Control Plans, PPAP) as site processes evolve.
• Assist in strengthening product audit systems, surveillance methodologies, and supporting data processes as the site's quality systems mature.
• Work effectively within ERP/SAP-type environments and evolving digital quality systems; contribute practical input that improves process controls, data visibility, and sustainable improvements.
Customer & Supplier Support
Provide audit findings and product build insights to Customer Quality and Production leadership as needed.
• Support customer and supplier audits by supplying technical data and build insights.
• Assist Supplier Development Engineering in resolving vendor discrepancies when required.
What Success Looks Like (12 Months)
• Reduced scrap and cost of poor quality through proactive intervention.
• Matured and expanded product surveillance program across key revenue parts.
• Established credibility and trust across manufacturing cells.
• Demonstrated sound judgment in connecting product and process observations to broader quality risks and improvement opportunities.
• Successfully exercised stop-work authority when required while maintaining credibility, trust, and a coach-oriented partnership with manufacturing teams.
Qualifications
Required
• 5+ years of experience in a manufacturing quality environment.
• Aerospace manufacturing experience.
• Hands-on experience with AS9102 First Article Inspection (FAI) and parts inspection activities.
• Demonstrated ability to independently conduct product and/or process audits with minimal oversight.
• Working experience participating in root cause analysis and corrective action activities in a production environment (e.g., 5-Why, Fishbone, 8D).
• Basic working knowledge of GD&T, manufacturing inspection principles, measurement tools, and quality documentation.
• Working proficiency with quality data analysis and common business systems, including Excel and ERP/SAP-type environments; ability to navigate Power BI or similar reporting tools.
• Ability to operate with authority and influence on the manufacturing floor while remaining approachable, tactful, and coach-oriented.
• Strong written and verbal communication skills, including the ability to clearly communicate audit findings to operators, supervisors, engineers, and leadership.
Preferred
• AS9100 audit experience or working knowledge of AS9100 requirements.
• Exposure to APQP tools (PFMEA, Control Plans, PPAP).
• Six Sigma training or certification.
• ASQ certification or experience in high-reliability / regulated manufacturing environments.
Education
• Bachelor's degree in engineering or a related technical field preferred; not required.
• Equivalent manufacturing quality experience will be considered in lieu of formal education.
Work Environment & Expectations
• Roving presence across manufacturing cells.
• High floor engagement and real-time interaction with build activities.
• Fully onsite, five-day workweek aligned to manufacturing operations.
• Specific daily hours may vary based on production needs and required floor coverage.
• Salary exempt position.
• Due to U.S. Government contract requirements applicable to this position, only U.S. citizens are eligible for employment in this role.
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