Senior Manufacturing Quality Engineer

September 16

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CHEP

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Global leader in pallet and container pooling services • Supply Chain Partner • Pallets • Containers • Automotive

10,000+

Description

• As a Manufacturing Quality Engineer at CHEP, you will be instrumental in ensuring the quality and reliability of equipment for future automated solutions in our global manufacturing process. • Collaborating closely with cross-functional teams, you will identify opportunities for process improvement, implement robust quality assurance measures, and drive continuous improvement initiatives to enhance equipment quality and end-user customer satisfaction. • This role will be responsible to lead detailed technical reviews regarding quality requirements for all future equipment in development. • Develop and implement quality assurance procedures and processes to ensure compliance with quality standards, regulations, and CHEP requirements throughout the manufacturing process. • Identify opportunities for process improvement in manufacturing operations, including assembly, machining, and testing processes, and implement corrective actions to enhance process/product quality and efficiency. • Conduct root cause analysis investigations to identify the underlying causes of quality issues and non-conformances and implement corrective and preventive actions to address them. • Utilize statistical analysis tools and techniques to analyse manufacturing data, identify trends, and make data-driven decisions to improve product quality and process performance. • Work closely with suppliers to ensure the quality and reliability of future automation and processes, conduct supplier audits, and implement supplier quality improvement initiatives as needed. • Establish and maintain quality control processes and inspection procedures to verify system conformance and ensure compliance with CHEP specifications and standards. • Maintain accurate and up-to-date documentation of quality processes, procedures, and records, and prepare reports and presentations to communicate quality performance metrics and improvement initiatives to stakeholders.

Requirements

• Minimum Bachelor's or Master’s degree, in Engineering, Quality Assurance, or a related field. • CQE certification or equivalent relevant experience • Background in manufacturing or industrial engineering, with a focus on quality equipment design and production. • Extensive experience in defining, implementing, and maintaining global Manufacturing Quality Management Systems (QMS), including Standard Operating Procedures (SOPs) and Test Protocols (TPs), ensuring compliance with industry standards and regulatory requirements. • Strong knowledge of quality management systems, methodologies, and tools, such as ISO 9001, Six Sigma, Lean Manufacturing, and Statistical Process Control (SPC). • Experience with root cause analysis techniques, such as 5 Whys, Fishbone diagrams, and Failure Mode and Effects Analysis (FMEA). • Proficiency in statistical analysis software such as Minitab, JMP, or Excel for data analysis and interpretation. • Proven ability to collaborate effectively with existing Quality organizations, leveraging expertise to mediate and drive necessary changes to current Pharmaceutical Quality Systems (PQS) in alignment with new automation processes, fostering a culture of continuous improvement and operational excellence. • Excellent problem-solving skills and the ability to work collaboratively with cross-functional teams to resolve quality issues and drive continuous improvement. • Strong communication and interpersonal skills, with the ability to effectively communicate technical information to stakeholders at all levels of the organization. • Experience working in a global or multinational environment, with exposure to diverse cultures and business practices.