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OSI Systems

Diversified tech company spanning security, healthcare

Supplier Quality Engineer

Validation, Compliance & Quality SystemsPosted on Nov 11
Full-timeBatam, Batam City, Riau Islands, IndonesiaNo salary listedIn-person

About the Job

Requirements

  • A bachelor's degree in Engineering, Quality Management, Manufacturing Technology, Business Administration, Supply Chain Management, or a related field is required.
  • At least three years of experience in supplier quality, quality systems, document control, quality assurance administration, and regulatory compliance support is required.
  • Knowledge of document control management, including maintaining controlled records, procedures, templates, and compliance documentation, is required.
  • Experience with supplier qualification processes, including supplier onboarding, risk assessments, capability reviews, approvals, and periodic reevaluations, is required.
  • Experience administering supplier audits, including audit scheduling, documentation requests, audit records, corrective action follow-up, and status tracking, is required.
  • Experience managing supplier scorecards, supplier performance metrics, KPI reporting, and related performance review documentation is required.
  • Ability to collect, analyze, and report quality data and key performance indicators to support supplier performance monitoring and continuous improvement is required.
  • Proficiency with Microsoft Office Suite, including Excel, Word, PowerPoint, and Outlook, is required.

Responsibilities

  • Manage supplier qualification files and records for all company locations.
  • Manage supplier quality documentation within the D365 ERP system.
  • Maintain quality agreements, certifications, audit reports, and supplier qualification records.
  • Ensure supplier records remain current and compliant with internal procedures and customer requirements.
  • Coordinate periodic reviews of supplier documentation.
  • Archive and store supplier records in accordance with company retention policies.
  • Support the Approved Supplier List (ASL) for various locations.
  • Coordinate supplier approval, conditional approval, suspension, and disqualification activities.
  • Update supplier approval status based on audit results, performance reviews, and management decisions.
  • Compile supplier approval reports for site and corporate management.
  • Verify that supplier certifications and regulatory registrations remain valid.
  • Coordinate supplier onboarding and qualification activities.
  • Manage supplier surveys, risk assessments, capability assessments, and qualification packages.
  • Monitor qualification progress and obtain necessary approvals.
  • Support periodic supplier re-qualification and re-evaluation activities.
  • Ensure qualification documentation is complete before granting supplier approval.
  • Manage supplier quality scorecards and KPI dashboards.
  • Collect quality and delivery performance data from various locations.
  • Prepare monthly and quarterly supplier performance reports.
  • Support supplier review meetings by providing performance metrics and data analysis.
  • Monitor supplier quality trends and escalation activities.
  • Support implementation of standardized supplier quality processes across locations.
  • Manage standardized templates, forms, procedures, and work instructions.
  • Coordinate supplier quality documentation harmonization projects.
  • Assist the site during internal, customer, and certification audits.
  • Ensure supplier quality records support compliance with ISO 9001, AS9100, ISO 13485, and IATF 16949 standards.
  • Support audit preparation and requests for supplier documentation.
  • Report quality problems or defects to a manager or senior management member so corrective action can be implemented and recurrence prevented.
  • Perform other duties as assigned to meet business needs.

Desired Qualifications

  • Experience working within a multi-site manufacturing environment is desired.
  • Experience in electronics manufacturing services (EMS) or a related electronics manufacturing environment is desired.
  • Ability to support supplier quality, quality systems, or compliance activities in aerospace, medical device, defense, or other regulated industries is a plus.

About the Company

OSI Systems

Diversified tech company spanning security, healthcare

OSI Systems operates three divisions: Security, Healthcare, and Optoelectronics and Manufacturing. The Security division supplies inspection systems for airports, ports, and borders that scan people and cargo using imaging and sensors. The Healthcare division produces patient monitoring and diagnostic equipment, while the Optoelectronics division makes electronic components for various devices. The company differentiates itself through its diversified, three-pronged portfolio and growth via acquisitions like Rapiscan and Spacelabs; its goal is to deliver technology-enabled solutions that protect people and infrastructure, support clinical care, and provide high-quality components.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Hawthorne, CA
Founded
1987

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