Verify system backup availability, project file backup status, and maintenance records.
Carry out basic inspection of PLC CPU/module status, I/O modules, communication modules, network switches, fibre links, power supplies, UPS, and panel condition.
Support functional checks on HMI graphics, alarm pages, trends, reports, client-server communication, and operator interface functions.
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Ensure the proper documentation, review, and approval of qualification and validation deliverables, such as risk assessments, traceability matrices, test scripts, deviations, and summary reports
Conduct periodic reviews of validated systems and perform re-validation as necessary.
Identify and drive continuous improvement initiatives and projects to enhance the qualification and validation efficiency and effectiveness fostering a culture of continuous improvement
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Works with Silicon Validation team to help set up various systems and infrastructure to support bring up of new and existing programs. Includes imagining HDD with the latest Windows or Linux images, collecting HW or SW to assist the various team or other lab duties as needed.
Perform or coordinate the implementation of Lab equipment Maintenance on Thermal heads, Chillers Scope or Analyzer Calibration and maintain the SCBU Margin Silicon environment
Perform or coordinate motherboard reworks and ASIC direct mount activity (in house and external) which includes collecting and providing motherboards to the External teams, creating support tickets, communicating directions and schedules to both external team and the requestor, provide status updates and then distribute complete reworks back to the requestors.
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- Minimum 2–3 years of relevant experience in validation, quality assurance, quality engineering, CAPA management, manufacturing engineering, or a related technical field. - Bachelor’s degree in Engineering, Science, Quality Management, or an equivalent technical discipline. - Experience in planning, executing, documenting, and reviewing validation activities for equipment, processes, systems, software, or products. - Experience in investigating non conformances, deviations, customer complaints, audit findings, quality issues and change management. - Knowledge of validation principles, CAPA processes, root cause analysis tools, risk management, and continuous improvement methodologies. - Familiarity with quality management systems and applicable regulatory or industry standards is preferred. - Knowledge of Good Documentation Practices (GDP) and data integrity principles. - Strong analytical, problem-solving, communication, and documentation skills. - Familiarity with quality management systems ISO 13485 and applicable regulatory or industry standards is preferred.