✦ Luna Orbit — Business Analysis

Quality Engineer II

at Owens & Minor

📍 Toano, VA Unknown 💰 $70K – $75K USD / year Posted March 26, 2026
Salary $70K – $75K USD / year
Type Not Specified
Experience mid
Exp. Years Not specified
Education Not specified
Category Business Analysis

This role involves managing validation programs to ensure sterility and quality standards in healthcare products. The engineer will oversee equipment and process validation, maintaining compliance and quality assurance.

  • Manage validation programs
  • Ensure sterility compliance
  • Oversee equipment and process validation
  • Maintain documentation
  • Collaborate with quality teams

Focus on validation of equipment, processes, and software related to sterilization, with expertise in quality management systems and healthcare standards.

The ideal candidate is a mid-level quality engineer or scientist with experience in validation and sterility assurance within healthcare or medical device industries. Strong analytical and problem-solving skills are essential.

Engineering or scientific expertiseValidation program managementQuality system knowledgeSterility assuranceProcess and equipment validation
Regulatory complianceGMPISO standardsHealthcare industry experience
Validation softwareQuality management systems
validation programsequipment validationprocess validationsoftware validationsterility assurancequality system management
Quality system managementSterility assuranceValidation programsEquipment validationProcess validationSoftware validationTerminal sterilizationSupplier qualityCAPADocument controlRisk managementSterilization standardsValidation management
LeadershipAnalytical thinkingProblem solvingAttention to detailCollaboration
Industry Healthcare
Job Function Ensure product sterility and quality through validation and compliance management
Role Subtype Validation Engineer
Tech Domains Validation software, Quality management systems
Clearance Required None
Visa Sponsorship No
quality systemsterility assurancevalidation programsequipment validationprocess validationsoftware validationterminal sterilizationsupplier qualityCAPAdocument controlrisk managementISO standardsGMPvalidation managementhealthcaremedical devicesvalidation

Lack of validation experience, No healthcare or medical device background, No understanding of sterilization processes, No scientific or engineering degree

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