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Quality Control Engineer
Quality Control EngineerClinLab Staffing • Clifton, NJ, US
Quality Control Engineer

Quality Control Engineer

ClinLab Staffing • Clifton, NJ, US
10 hours ago
Job type
  • Full-time
Job description

Base pay range

$90,000.00 / yr - $120,000.00 / yr

Scientific Recruiter focusing in NY, NJ, PA, MD, and DE

Mission

To uphold and advance the highest standards of quality across all stages of manufacturing—ensuring compliance with AS9100 and customer-specific requirements through robust documentation, risk management, and process validation. This role exists to proactively prevent quality issues, support internal and customer-facing investigations, and strengthen our reputation as a trusted partner for mission-critical components.

Competencies – What This Person Must Be

  • Standards-Driven : Understands and applies AS9100, ISO 9001, MIL-STD-1916 and customer-specific standards; ensures audits, validations, and ongoing operations meet all requirements.
  • Root Cause Problem Solver : Leads investigations using 8D, 5 Whys, and Ishikawa methods to ensure sustainable corrective actions.
  • Process Control Advocate : Uses SPC, PFMEA, control plans, and capability studies to ensure consistent, capable production.
  • Metrics-Driven : Uses data analysis to monitor trends, reduce scrap, and eliminate recurrence of quality issues.
  • Customer-Focused : Communicates clearly with aerospace, defense, and other high-stakes clients; drives issues to closure and delivers timely updates.
  • Cross-Functional Collaborator : Partners with Engineering, Manufacturing, and Production teams to align on requirements, validate processes, and resolve issues quickly.
  • Detail-Oriented : Manages documentation and compliance requirements with accuracy including FAIRs, PPAPs, CAPA records, SOPs, and quality alerts with full traceability.
  • Self-Directed and Proactive : Takes initiative to identify and resolve quality risks without being prompted and with minimal supervision; follows through on actions with rigor and accountability.

Key Responsibilities

  • Drive quality improvements through Gage R&R studies, Statistical Process Control (SPC), Six Sigma, and Lean Manufacturing tools.
  • Lead investigations into internal and external quality issues; document findings and ensure timely resolution.
  • Perform root cause analysis using structured problem-solving methods (8D, 5 Whys) and verify the effectiveness of corrective and preventive actions (CAPA).
  • Coordinate timely responses to Supplier Corrective Action Requests (SCAR), Non-Conformance Reports (NCR), customer complaints, and quality-related queries.
  • Prepare and maintain First Article Inspection Reports (AS9102), Production Part Approval Process (PPAP-AS9145) documentation, and validation (IQ / OQ / PQ).
  • Lead risk assessments (PFMEA) and develop control plans to mitigate quality risks.
  • Track and analyze defects and scrap data to identify trends and prioritize corrective actions.
  • Collaborate with manufacturing and engineering to improve processes and define inspection criteria.
  • Own inspection processes, including CMM (Zeiss – Calypso), OGP, and Keyence programming, as well as inspection fixture design (SolidWorks preferred).
  • Oversee QC personnel training in partnership with manufacturing engineering to establish visual standards and develop work instructions.
  • Maintain SOPs, work instructions, inspection procedures, and training logs in compliance with AS9100.
  • Support internal, customer, and regulatory audits, ensuring readiness and compliance.
  • Key Metrics & KPIs

  • = 95% On-Time Submission of FAIRs, PPAPs, SCAR's, and CAPA's
  • Required Experience And Qualifications (Subject To Management Discretion)

  • Bachelor's degree in Mechanical, Manufacturing, or a related Engineering field
  • 3–5+ years of quality engineering experience in injection molding or precision manufacturing
  • Working knowledge of AS9100, ISO 9001, and MIL-STD-1916
  • Experience with FAIR, PPAP, SPC, PFMEA, control plans, and CAD (SolidWorks preferred)
  • Proficiency in statistical tools (Minitab, JMP, Excel) and QMS / ERP systems
  • Strong written and verbal communication skills
  • Preferred Qualifications

  • ASQ Certified Quality Engineer (CQE) or Six Sigma certification
  • Experience in the defense, aerospace, or medical device industries
  • Hands-on inspection experience, including CMM, optical, or non-contact methods
  • Experience with CMM programming and operation (Zeiss – Calypso)
  • Physical Requirements

  • Ability to stand and walk on the production floor for extended periods
  • Capable of lifting up to 40 lbs and accessing production and inspection equipment
  • Manual dexterity for handling tools, parts, and inspection equipment
  • Visual acuity sufficient to read prints, inspect parts, and identify quality defects
  • Tolerance for a manufacturing environment with heat, noise, and moving equipment
  • Manufacturing facility with exposure to injection molding machines, CNC equipment, and secondary operations
  • Requires use of PPE, including safety glasses, gloves, and hearing protection
  • Frequent collaboration with production, maintenance, and engineering teams on the floor
  • Seniority level

  • Associate
  • Employment type

  • Full-time
  • Job function

  • Engineering and Quality Assurance
  • Industries

  • Manufacturing, Aviation and Aerospace Component Manufacturing, and Medical Equipment Manufacturing
  • Referrals increase your chances of interviewing at ClinLab Staffing by 2x

    Inferred from the description for this job

    Medical insurance

    Vision insurance

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