✦ Luna Orbit — Engineering (Non-Software)

Product Quality Engineer

at Dover

📍 Salem, NH, US, 03079 Hybrid 💰 $72K – $108K USD / year Posted March 13, 2026
Salary $72K – $108K USD / year
Type Not Specified
Experience mid
Exp. Years Not specified
Education Not specified
Category Engineering (Non-Software)

The Product Quality Engineer supports quality improvement initiatives, ensures compliance with standards, and collaborates across departments to maintain product quality throughout the lifecycle.

  • Support quality initiatives
  • Review process compliance
  • Conduct root cause analysis
  • Manage CAPA and non-conformances
  • Support audits

This role involves applying quality engineering tools, standards like ISO and ASTM, risk management, and process validation techniques within a manufacturing environment.

The ideal candidate is a mid-level quality engineer with experience in manufacturing quality standards, risk management, and process validation. They possess strong problem-solving skills and familiarity with ISO, ASTM, and regulatory compliance requirements.

Quality EngineeringISORisk managementProcess validationCAPARoot cause analysis
Six SigmaLean TechniquesFDAEU machine directiveRegulatory standards
ISO standardsASTM standardsFDA standardsEU machine directive
Quality EngineeringISOTSASTMMachine directiveRisk managementPDCASix SigmaKaizenLeanProcess validationCAPARoot cause analysisRegulatory complianceProduct lifecycle management
Quality EngineeringISOTSASTMMachine directiveRisk managementPDCASix SigmaKaizenLeanProcess validationCAPARoot cause analysisRegulatory complianceProduct lifecycle management
Problem-solvingAnalytical thinkingCollaborationCommunicationAttention to detail
Industry Manufacturing
Job Function Ensure product and process quality compliance in manufacturing
Quality EngineeringISOTSASTMMachine directiveRisk managementPDCASix SigmaKaizenLeanProcess validationCAPARoot cause analysisRegulatory complianceProduct lifecycle managementFDAEU machine directive

Lack of experience with ISO/TS/ASTM standards, No background in risk management or process validation, Unfamiliarity with regulatory standards like FDA or EU directives

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