Coordinate all activities for identification, collection, indexing filling and storage related to the Document Control procedure, including QC documents. (E.g. CPIS, DR, RIR)
Input document data into the standard registers ensuring that the information is accurate and up to date.
Maintain updates records of all approved documents.
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Coordinate and monitor Corrective and Preventive Actions (CAPA).
Review and approve quality documents including SOPs, work instructions, inspection standards, validation protocols, and engineering change documentation.
Support internal, supplier, and external audits, including customer and regulatory inspections.
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Apply established Manufacturing QA standards, methods, playbooks and tools to support consistency, standardization and adoption of proven approaches across manufacturing teams.
Use quality and manufacturing data, including NCP/CAPA learning, validation outputs, audit findings and process performance signals, to identify trends, support investigations, recommend preventive actions and contribute learning to future Quality Engineering solutions.
Contribute to continuous improvement of manufacturing quality systems, processes and engineering practices, supporting improved Right First Time performance and reduction of repeat or systemic quality issues.
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· Maintain and control QA/QC practices with regular checks and inspections ensuring correct operation and implementation of procedures.
· Develop and determine all standards to perform inspection and tests on all procedures and oversee all testing methods and maintain high standards of quality for all processes.
· Accountable for the quality and workmanship of site activity, good knowledge of all aspects of engineering construction relating to architectural and structural discipline interfacing the multidisciplinary processes.
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