Quality Engineering Technician- 2nd Shift in Scranton, Pennsylvania at Noble Biomaterials

Join a Team That Makes a Difference!

At Noble, the work you do matters. We manufacture innovative products that support the military, advance the medical field, and improve everyday life. Whether it's enhancing safety, enabling critical care, or solving real-world challenges, our solutions help people when it matters most. Be part of a purpose-driven team where your skills contribute to meaningful change. Noble Biomaterials, Inc is currently seeking a Quality Engineering Technician on our 2nd shift (12pm-8pm). The Quality Engineering Technician (QA Technician) is a hands-on, manufacturing-focused quality role that provides real-time support to daily production operations. This position is embedded on the production floor and partners closely with Fabric Operations, Process Engineering, and Production to reinforce quality procedures, support inspection and disposition decisions, and ensure accurate and compliant documentation. This role is critical to supporting the expansion to two-shift fabric manufacturing and serves as the primary quality presence on the production floor during second shift. This is not a laboratory role—the focus is on manufacturing execution, quality discipline, and operational decision-making.

What You’ll Do:

Serve as the primary Quality Assurance representative on the production floor during second shift.Support fabric inspection activities, including visual inspections, in-process checks, and disposition decisions in accordance with approved procedures and specifications.Partner with the Fabric Quality Engineer, QE Manager, Operations, and Process Engineering on day-to-day quality decisions.Reinforce adherence to approved work instructions, control plans, and standard operating procedures (SOPs).Monitor quality performance trends and assist with root cause analysis and failure investigations.Utilize quality tools (InfinityQS, JMP, Decision Logs) to analyze performance trends and document deviations.

Documentation & Good Documentation Practices (GDP)

Ensure accurate, complete, and timely completion of batch records, travelers, inspection records, and manufacturing documentation in compliance with GDP requirements.Review documentation for accuracy, completeness, and compliance prior to escalation or release.Verify that process documentation reflects current manufacturing practices and escalate discrepancies as needed.

Operational & Cross-Functional Support

Support Operations and Process Engineering with real-time issue identification, containment actions, and production floor feedback.Assist with the implementation and reinforcement of approved process changes and procedural updates.Act as a quality liaison between shifts to ensure continuity of communication, issues, and corrective actions.

Continuous Improvement & Compliance

Identify quality risks, recurring issues, and gaps in procedural adherence; escalate appropriately.Support internal audits, inspections, and quality initiatives.Promote a strong quality culture through visibility, clear communication, and consistent expectations.

Additional Responsibilities

Perform other related duties as assigned by Quality or Operations management.