Cyrus Technology started in 2005 with the vision to approach polymeric tooling design in unconventional methods and providing manufacturing solutions to exacting specifications for ultra-precision and complex moulding. We pride ourselves as a valued partner to our clients, offering expertise at every stage of the product design to manufacturing, to transform market opportunity ideas to a marketable product. With the progress we achieved so far, we aim to continue to push boundaries and overcome constraints to be a leader in the industry.
About the Job
The Quality Department plays a very important role in Cyrus in maintaining the quality management system and driving quality improvements to deliver high quality products for our customers. You will be working closely with the Assistant Quality Manager on Quality Management System (QMS) and suppliers' management.
Your key responsibilities are as follows:
- Maintain updated and accurate documents and records on ISO 9001, 14001 and 13485 system (includes Quality Manual, Procedures, Work Instructions, Forms, etc.) to ensure system compliance and ready for Management Review.
- Plan and conduct internal and external audits to ensure readiness of all sections for third party certification body, management review and customer audits.
- Coordinate with internal stakeholders to participate in customer or supplier audits for compliance
- Review audit findings and develop action plans to drive continuous improvements.
- Generate and review quality reports on suppliers' performance and work with suppliers to address non-conforming materials, and drive for continuous improvement.
- Issue and follow up on Supplier Corrective Action Request (SCAR) to suppliers, monitor and review SCAR effectiveness for timely closure.
- Support the qualification of new suppliers to maintain a healthy pipeline of qualified suppliers to meet Cyrus production requirements.
- Maintain and conduct regular review of calibration and preventive maintenance for equipment.
- Responsible for quality issues arising from production and customer feedback, and collaborate with the production team to address internal process issues and implement corrective actions to resolve customer complaints with proper documentation.
- Responsible for timely closure of Corrective and Preventive Actions (CAPA), non-conformance investigation report and customer complaints and, publish reports on quality performance.
- Lead the Material Review Board (MRB) meeting involving members from production, engineering and quality departments to conduct root cause analysis, address quality issues, implement corrective actions and review its effectiveness.
- Lead the team of QC inspectors in the inspection of parts for conformity in accordance with relevant drawing requirements.
Your areas of knowledge and expertise
that matter most for this role:
Diploma in quality management / Engineering / Manufacturing or related field
Minimum 3 to 5 years of relevant working experience in handling audits and ISO documentation in manufacturing industries.
Knowledge in Supplier Management
Knowledge of quality Management Standards such as ISO 9001, 14001, 13485 and ISO 22301.
Knowledge in Potential Failure Mode Effect Analysis (PFMEA), Control Plans .and Gage Repeatability & Reproducibility (GR&R)
Familiar with 8D and 5W problem solving methodology.
Good communication and presentation skills
Organized and detail oriented.
Positive attitude with ability to multi task.
Independent, takes initiatives and able to work with minimum supervision.
Good team player with good initiatives and ability to work independently.
Job Types: Full-time, Permanent
Pay: $3,000.00 - $4,000.00 per month
Benefits:
Free parking
Health insurance
Education:
Local Polytechnic Diploma (Preferred)
Experience:
Quality assurance: 4 years (Preferred)
Work Location: In person
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