Senior Quality & Compliance Systems Analyst

Support Revolution

's-Hertogenbosch

On-site

EUR 70,000 - 110,000

Full time

14 days+

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Job summary

Supermicro is seeking a Quality Systems Analyst to lead IMS, QMS, EMS and ISMS across the site, aligning with ISO 9001, 13485, 14001, 27001 requirements. You will develop, train, deploy, audit and maintain documentation, and drive continual improvement.

You will coordinate internal and external audits, manage KPIs, and serve as subject matter expert on IMS standards, ensuring compliance with regulatory and customer expectations in a high‑tech manufacturing setting.

Qualifications

  • Bachelor's degree in Engineering, Quality Management, Environmental Science, or related field.
  • 5+ years in Quality/Environmental/Management Systems in manufacturing/high-tech.
  • Experience auditing IMS in semiconductor/electronics/pharma/medical device.
  • Strong knowledge of ISO 9001, 13485, 14001, 27001, AS9100, and IATF 16949.
  • Certified Internal Auditor preferred.
  • Excellent communication and collaboration skills.

Responsibilities

  • Plan, conduct, report internal audits and close corrective actions.
  • Develop and maintain QPs, WIPs, SOPs and IMS documents.
  • Review change requests and monitor KPIs.
  • Lead improvement initiatives for IMS effectiveness.
  • Coordinate audits with certification bodies and regulators.
  • Provide training on IMS requirements.
  • Serve as IMS subject matter expert across the org.
  • Keep current with ISO standards and regulatory requirements.
  • Escalate compliance risks to management.
  • Execute special projects as assigned.

Skills

Auditing expertise
Documentation control
Regulatory compliance

Education

Bachelor's degree in Engineering, Quality Management, Environmental Science, or related field
Master's degree preferred

Job description

Supermicro is seeking a Quality Systems Analyst to lead IMS, QMS, EMS and ISMS across the site, aligning with ISO 9001, 13485, 14001, 27001 requirements. You will develop, train, deploy, audit and maintain documentation, and drive continual improvement.

You will coordinate internal and external audits, manage KPIs, and serve as subject matter expert on IMS standards, ensuring compliance with regulatory and customer expectations in a high‑tech manufacturing setting.

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