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Super Micro Computer Spain, S.L. · 1 month ago

Quality Systems Analyst

San Jose, CA

Full-time

Onsite

Entry, Mid Level

$69K/yr - $74K/yr

2+ years exp

Supermicro is a Top Tier provider of advanced server, storage, and networking solutions. The Quality Systems Analyst will support the development and implementation of Quality Management Systems, Environmental Management Systems, and Information Security Management Systems, ensuring compliance with ISO standards.

Data StorageInternet of ThingsNetwork HardwareSoftware

Responsibilities

Support the implementation, maintenance and improvement of the QMS, EMS, ISM, procedures and department specific processes

Plan, perform, assist in company-wide internal audit program, from planning, implementation, report generation, corrective action issuance, verification and closure

Support external audits by the Notified Body, other regulatory bodies and third-party auditors

Day-to-day management of the local ISO related activities and projects, including but not limited to the following

Work closely with all departments in regard to ISO implementation, issues, maintenance and improvement activities

Coordinate appropriate and effective corrective and preventive (CAPA) actions in response to pertinent observations and findings from the audit program, external regulatory agency inspections, customer complaints and other internal / external non-conformances

Document Control activities through the automated documentation system including training of associates to read, review and approve documents; and maintaining a fully compliant system

Detailed review of ISO controlled documents in order to ensure its adequacy

Assists in the gathering, trending and reporting of performance indicators and reporting the status to management

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

Support the development of requirements, validation and implementation of automation projects to optimize the effectiveness of the QMS, EMS and ISM

Execute and complete projects and other duties as assigned

Qualification

ISO StandardsQuality Management SystemEnvironmental Management SystemInternal AuditsRisk ManagementData AnalysisMulti-tasking SkillsInfluence ManagementCommunication SkillsOrganizational Skills

Required

Bachelor's degree in related field required

Working knowledge of ISO International Standards, such as ISO 9001, 13485, 14001, 27001, AS9100, TS16949, etc

Influence management skills; demonstrated ability to work constructively across all functions of the organization, including with customers and suppliers

Strong communication and presentations skills (articulate and persuasive)

Sound organizational and multi-tasking skills

Strong computer and analytical skills, including data analysis and reporting using, Microsoft Excel, Access, Word, PowerPoint, Outlook, etc

Knowledge of Risk Management (risk assessment tools such as FMEA, fault tree, etc.) and KPI (Key Process indicators)

Fast-paced office environment; requires significant use of telephone and computer keyboard, monitor, and mouse

May require domestic and international travel (10-20%)

Preferred

minimum 2 years of relevant experience in quality system with experience in manufacturing and / or high-tech industry

Experience in developing and leading quality and environmental management system audits in the semiconductor / electronics manufacturing, pharmaceutical or medical device industries