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Super Micro Computer Spain, S.L. · 2 months ago

Quality System Manager- ISO (26953)

San Jose, CA

Full-time

Onsite

Senior Level, Lead/Staff

$115K/yr - $135K/yr

8+ years exp

Supermicro is a leading innovator in high-performance server technology, providing solutions for various sectors including Data Center and Cloud Computing. The Quality System Manager will oversee the development and implementation of Quality Management Systems in compliance with ISO standards, ensuring effective processes and compliance through audits and training.

Data StorageInternet of ThingsNetwork HardwareSoftware

Responsibilities

Provide support to internal functions in the application, maintenance and improvement of quality systems, procedures and department specific processes

Coordinate external audits by the Notified Body, other regulatory bodies and third parties, and coordinates responses to applicable audit findings

Prepare performance reports and metrics for the QMS, EMS and ISM

Ensure efficient and effective processes and tools are established for compliance with ISO standards requirements

Serve as the process owner and subject matter expert for key elements of the QMS, EMS and ISM, including CAPA, Complaint Handling and Internal Audit

Lead / participate in company-wide internal audit program including planning, implementation, report generation, corrective action issuance to closure

Conduct local and global training on key elements of the QMS, EMS and ISM, including CAPA, Complaint and Internal Audit

Execute projects and complete other duties as assigned

Qualification

ISO 9001ISO 13485ISO 14001ISO 27001Quality Management SystemsEnvironmental Management SystemsInformation Security ManagementRisk assessment methodologiesMulti-tasking skillsLeadership skillsCommunication skillsOrganizational skills

Required

Bachelor's degree in General Business, Engineering, Science, or a related field

Minimum of 8 years of working experience in a relevant quality or compliance-related field, with at least 5 years of direct experience managing Quality / Environmental Management Systems (Q/EMS)

Proven experience in developing and managing QMS, EMS, and ISMS within manufacturing, electronics, semiconductor, pharmaceutical, or medical device industries

Strong knowledge and practical application of ISO and international standards, including but not limited to: ISO 9001 (Quality Management), ISO 13485 (Medical Devices), ISO 14001 (Environmental Management), ISO 27001 (Information Security), AS9100 (Aerospace Quality Systems)

Demonstrated influence management skills, with the ability to collaborate effectively across departments, and engage with both customers and suppliers

Excellent communication and presentation skills – confident, articulate, and persuasive in both verbal and written formats

Proven leadership and team management abilities, including: Developing and executing strategic plans, Defining clear roles, responsibilities, and performance expectations, Providing hands-on support when needed (e.g., conducting audits, leading process reviews)

Strong organizational and multi-tasking skills

Working knowledge and practical application of risk assessment methodologies (e.g., FMEA) and key performance indicators (KPIs) for process monitoring and improvement

Willingness to travel as needed; 10–20% domestic and/or international travel may be required