DQE - AV&I Professional

Job description

Job Title DQE - AV&I Job Description **Job Title : DQE - AV&I** The Senior Design Assurance Engineer will support design controls and quality management associated with the development, transfer and sustaining initiatives for the medical devices. **You are responsible** - Lead all quality elements of Design Controls and product Design History Files. - Drive Quality norms associated with design engineering projects. - Support integration of Risk Management processes throughout the product lifecycle from initial development through post market surveillance in accordance with Philips processes and global standards. - Lead Quality Plan initiatives associated with Risk Management and Quality System integration. - Support integration of post market surveillance processes into Design Controls and Sustaining initiatives through analysis of field performance, identification of trends and risks, and actions to eliminate or mitigate adverse post market issues. - Support the Regulatory Affairs department for submissions and respond to submission questions. - Lead and support Corrective and Preventive Actions (CAPA) and QMS continuous improvement initiatives. - Analyze situations/data using engineering principles and collaboration to identify gaps between project work and QMS. - Transfer Quality deliverables for new products and sustaining projects to manufacturing and operations quality and supplier quality teams. - Support internal and external audits. - Acts in full compliance to all applicable regulatory requirements and Philips Quality policies. **Minimum required Education:** Bachelors / Masters Degree in Mechanical Engineering, Electronics Engineering, Science or equivalent. **Minimum required Experience:** Minimum 8-10 years of experience with Bachelors/Masters in areas such as Quality Engineering, Safety Engineering, R&D Engineering or equivalent. **Preferred Certification:** Six Sigma Green Belt **Preferred Skills:** - Design Quality Management - Experience in ISO 14971, 21 CR 820, ISO 13485, EU MDR, IEC 60601-1, IEC 62366, and IEC 62304 standards - Mandatory - Data Analysis & Interpretation - Design for Quality (DFQ) - Root Cause Analysis (RCA) - CAPA Methodologies - Regulatory Requirements - Privacy, Safety and Security Risk Assessment - Technical Documentation - Continuous Improvement - Product Quality and Reliability - Product Lifecycle Management (PLM) - People Management - Defect Management - Design Verification Planning - Design Validation Planning - Product Test Design **How we work together** We believe that we are better together than apart. For our office-based teams, this means working in-person at least 3 days per week. Onsite roles require full-time presence in the company s facilities. Field roles are most effectively done outside of the company s main facilities, generally at the customers or suppliers locations. Indicate if this role is an office/field/onsite role. Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.