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Quality Manager

Job in East Providence, Providence County, Rhode Island, 02914, USA
Listing for: Quantic Electronics
Full Time position
Listed on 2026-03-12
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering, Quality Control / Manager, QA Specialist / Manager
  • Engineering
    Quality Engineering, QA Specialist / Manager
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below

Description

The Evans Capacitor Company is hiring! Evans currently has an opening for an on-site Quality Manager at its flagship facility located in East Providence, Rhode Island. Be part of the innovative teams supporting mission‑critical applications in the aerospace and defense, telecommunications and energy industries. Evans manufactures high‑energy density capacitors for demanding mission‑critical applications with two manufacturing facilities in East Providence, RI and Sanford, ME.

We have the most power dense capacitor technology in the industry and are routinely specified for defense, aerospace, and energy exploration applications where high reliability and SWaP (space, weight, and power) savings are critical design considerations.

Job Type

Full‑time

Key Responsibilities
  • Actively govern the Quality Management System (QMS) with retained authority over core policies, procedures, metrics, and controls; proactively facilitate cross‑functional teams to drive timely review, revision, approval, and release of all QMS documentation and processes—ensuring ongoing currency and full AS9100D compliance.
  • Ensure management reviews are planned, conducted, and documented in accordance with AS9100D requirements, focusing on QMS performance effectiveness, risks, opportunities, audit results, customer feedback, and continuous improvement actions, and ensuring resulting actions are assigned, tracked, and completed.
  • Ensure that quality planning, control, and verification activities are embedded and fully integrated into manufacturing and operational processes as essential components of the QMS, supporting effective operational planning and control in accordance with AS9100D requirements.
  • Actively govern and oversee the control of nonconforming outputs (including the Material Review Board [MRB] process), ensuring identification, segregation, timely evaluation, disposition, documentation, and linkage to systemic corrective actions to prevent recurrence—in full compliance with AS9100D requirements.
  • Lead and be accountable for the supplier corrective action process, including issuance of requests, verification and validation of supplier‑submitted root cause analyses, corrective actions, and effectiveness evidence, as well as tracking, approval, and closure to prevent recurrence; support the Purchasing group in supplier evaluations, performance monitoring, and flow‑down of quality requirements, while ensuring the quality team’s execution of incoming verification activities and risk mitigation for externally provided processes, products, and services—in full compliance with AS9100D Clause 8.4 requirements.
  • Serve as the primary quality interface for quality inquiries, corrective action responses, and support to the Customer Quality Manager on returned nonconforming product, ensuring timely, thorough, and effective resolution.
  • Apply root cause analysis, corrective and preventive action methodologies, and continuous improvement tools (e.g., Lean, Six Sigma) to address systemic quality issues and reduce risk.
  • Collaborate with Engineering, Operations, Supply Chain and Customer Quality to resolve quality issues, ensure process capability and verify equipment.
  • Ensure facility compliance with AS9100D, FAR, customer‑specific, and applicable regulatory requirements, maintaining audit‑ready documentation and objective evidence at all times.
  • Identify quality and operational risks using risk‑based thinking, implementing mitigation strategies across processes, suppliers, and information systems, including cybersecurity considerations related to CMMC.
Audits & Certifications
  • Plan, lead, execute, and report internal audits to verify QMS conformance and effectiveness across all applicable AS9100D and customer specific requirements.
  • Support external third‑party audits and assist the Customer Quality Manager during customer audits, ensuring effective preparation, evidence gathering, and timely response to findings.
  • Ensure timely and effective corrective actions are implemented, verified for effectiveness, and sustained.
  • Drive audit findings to closure with clear ownership, measurable actions, and management visibility.
Leadership & Team…
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