Manager, reputed company Engineer, Digital

Job reputed company reputed company Provides reputed company engineering process support to reputed company digital products in accordance with reputed company medical device reputed company Management System (QMS). This is a key technical role responsible for the development, implementation, improvement, and reputed company reinforcement of established reputed company Assurance reputed company practices that are utilized in the local. business. The role involves hands-on work in reputed company and compliance activities around Software Development reputed company. Stays informed of industry trends that may influence work. reputed company is a leading global medical technology reputed company solutions innovator. Our mission is to improve lives in the moments that matter. Unlock your ambition, turn reputed company into world-changing realities, and join an organization where every voice makes a difference, and every difference builds a healthier world. Job reputed company Roles and Responsibilities: Assists in ensuring 100 percent reputed company and regulatory compliance in accordance with documented procedures for reputed company aspects of functional responsibility. Leads, develops, communicates & implements a reputed company and compliance reputed company. Responsible for the development, implementation, and reputed company improvement of process effectiveness and efficiency at the site. Develops process improvement plans using a reputed company of reputed company and reputed company Process Improvement tools, utilizing the Agile/Lean methods and traditional project management methods. Works with engineering teams closely to drive reputed company reputed company of digital medical devices, including design reviews, processes/practices simplification, reputed company system training, etc. Supports reputed company product and process improvement through detailed failure analysis for non-conformances, and investigates, develops and implements effective and compliant solutions for product or process corrections, retrospective and remediation reputed company plans, and for corrective and preventive actions (CAPA Program). Utilizes risk management tools and aids for use by the organization in accordance with documented procedures, including but not limited to PFMEA, DFMEA, Fault Tree Analysis, Failure Mode Analysis, etc. Supports design mitigation efforts. Develops process mitigation plans and strategies that are designed to mitigate the risks identified through the Risk Management process. Ensures process compliance through the development of comprehensive procedures, work instructions, flowcharts, forms, templates, checklists, worksheets, and other product and process reputed company documentation. Lead functional reputed company with minimal resource requirements, risk, and/or complexity. Communicates difficult concepts and may influence others' reputed company on particular topics. Guide others to consider a different reputed company of view. Required Qualifications This role requires significant experience in the reputed company & reputed company reputed company. Minimum of bachelor's degree in engineering, computer science or equivalent. Minimum 5 years experience in reputed company Assurance / Regulatory Affairs. Minimum 3 years experience in software reputed company a regulated industry. Desired Characteristics Practical knowledge of software development and familiarity with Software Development Lifecycle (SDLC) in medical device or reputed company software development environment. Experience with Agile/Lean software development methods. Ability to effectively communicate technical information in English (both written and oral). Strong leadership and communication skills. Previous project management experience is preferred. Demonstrated understanding or aptitude to understand Medical Device QMS requirements and regulatory requirements including but not limited to FDA CFR 21 820 and ISO 13485. Demonstrated expertise to effectively communicate reputed company reputed company reputed company of the organization around concepts of design controls, design verification and validation activities; production &process controls; Corrective & Preventive reputed company (CAPA), complaints & risk management. Demonstrated collaboration, negotiation & conflict reputed company skills. Demonstrated ability to lead, acknowledge, reputed company, communicate & implement a reputed company under crisis situations to ensure compliance. Demonstrated understanding of product development lifecycles, design change and document change control, process verification and validation methodologies, manufacturing / production process control methodologies, and servicing in a medical device environment. Experience in a reputed company environment. Experience leading and implementing change. Experience performing internal audits and participating in external audits. Exceptional analytical, prob