Supplier Quality Engineer

Insulet; Gelang Patah; In loco; MYR 60.000 - 90.000; Tempo pieno

Descrizione del lavoro

Insulet Corporation in Malaysia seeks an Engineer, Supplier Quality to support supplier selection, qualification, and management, ensuring Insulet quality standards are met. You will work with suppliers and internal teams to communicate quality metrics and drive corrective actions.

Responsibilities include maintaining supplier records, auditing suppliers, CAPA initiation, and reporting supplier performance to management, while supporting Design Control and regulatory compliance with FDA/ISO

Competenze

• Bachelor's degree in science or engineering required.
• 2–5 years of quality/ supplier quality experience in medical devices.
• Experience with ISO 13485, FDA regulations and CAPA processes.
• Able to communicate across multiple levels with external partners.

Mansioni

• Support supplier selection, qualification, and management to meet Insulet requirements.
• Maintain supplier records and audit schedules; generate audit reports.
• Lead CAPA activities and drive corrective actions with suppliers.
• Communicate quality metrics via supplier scorecards and management reviews.
• Assist in internal audits and participate in design control initiatives.

Conoscenze

Quality Assurance

Supplier Quality

Auditing

Communication

Formazione

BS in Engineering

Strumenti

Microsoft Word

Microsoft Excel

PowerPoint

Outlook

Descrizione del lavoro

Job Summary

Responsibilities: Reporting directly to the Manager, Supplier Quality, the Engineer, Supplier Quality is responsible to support the selection, qualification, and management of suppliers. Closely works with suppliers to ensure product/service quality meets lnsulet requirements. Interfaces with other Insulet departments/functions as well as with suppliers and other external parties on issues related to product/service quality. Effectively communicates Quality metrics through supplier scorecards and Management Review to the organization, suppliers, and Executive Management.

• Maintain approved supplier list and supplier history records in accordance with quality system requirements.
• Assist with the qualification of new suppliers, new components, and changes by developing and executing, in conjunction with other internal groups, a robust and complete set of plans and requirements for such qualifications.
• Maintains accuracy of Supplier Audit Reports and Supplier Profile
• Develop and maintain the Supplier Audit Schedule to ensure supplier audits are scheduled per internal procedure.
• Plans and conducts scheduled audits of suppliers to assess compliance with lnsulet Requirements.
• Prepares Audit Reports to document audit findings and observations.
• Communicates quality issues to suppliers as needed and provides assistance to develop corrective actions.
• Initiate and follow up on supplier CAPA for both audit deficiencies and internal non-conformances to ensure timely closure and effectiveness.
• Generates Monthly/Quarterly and Annual Supplier Performance Reports for Management visibility.
• Tracks and trends supplier performance via supplier scorecards, taking remedial action as needed.
• Conduct and assist with internal audits.
• Assist or leads CAPA evaluation and closure as related to the supplier quality processes and or supplier performance.
• Participate in developmental and departmental training.
• Support Site during external audits (i.e. BSI, FDA, Customer).
• Performs other duties as required.

Requirements

• Bachelor's degree (preferably science or engineering discipline) required.
• 2 to 4 years of experience in quality in the medical device industry
• Fluent in both English and Malay language.
• Ability to communicate and work effectively at multiple levels within the organization and with external business partners.
• Good interpersonal skills in dealing with suppliers, peers and other functional areas.
• Working knowledge of ISO 13485 quality system standards
• Auditor training certification to ISO 13485, 17025 or other industry QMS Standard preferred.
• The ability to prioritize multiple competing deliverables simultaneously.
• Must be proficient in Word, Excel, Outlook and Power Point.

Position Overview

This position is responsible for Design Control to ensure current products and new projects meet the regulatory and quality requirements for medical devices. Interfaces with other Insulet departments (e.g. Sr. Management, Operations, and Information Technology, Engineering, New Business Development and Regulatory Affairs) as well as other external parties on issues related to product development and launched product support. Effectively communicate design and development regulations, optimizing development, review and/or approval of design documents and protocols and ensuring ambiguities and conflicting requirements are resolved are critical to the success of the position.

Responsibilities

• Responsible for Design Control initiatives to develop appropriate Design History File documents. Review and approve new product documentation, as required.
• Collaborate with Project Management to optimize Design Control process and develop Sustaining Quality Engineering process.
• Review and approve Design Control documents and protocols.
• Serve as the Design Control expert to organization.
• Develop and deliver Design control training for organization.
• Support CAPA activities
• Support Risk Management activities and ensure compliance to standards and regulation
• Performs other duties as assigned.

Education and Experience

Minimum Requirements:

• BS degree, in an engineering/scientific/computer systems/ or quality management curriculum or equivalent experience.
• A minimum of 2-5 years work experience in Quality Assurance within an FDA, ISO or other regulated environment and/or equivalent combination of education and experience.
• Experience in the development and implementation of effective Design Control Systems.
• Working knowledge of the Quality System Regulation (FDA 21 CFR Part 820), ISO 13485 Medical devices - Quality management systems, and ISO 14971 Medical devices - Application of risk management to medical devices.
• Working knowledge of EN 60601, Safety requirements for medical electrical systems.
• Working knowledge of ISO 62304, Medical Device Software - Software Life Cycle Process
• Fluent in computer skills, and at minimum, the use of Microsoft Office programs (e.