Job Overview: This is a career opportunity to work with a medical device manufacturer at the forefront of innovation. * We are seeking an experienced professional who can develop and implement quality management systems that meet regulatory requirements, ensure compliance, and drive business success. The ideal candidate will have strong problem-solving skills, be results-driven with attention to detail and excellent communication skills. Key Responsibilities: • Develop and continuously improve compliant quality management systems. • Plan and coordinate internal audits to verify compliance. • Manage documentation related to product design control and risk analysis • Ensure effective technical regulation documentation for manufacturing processes including test methods plans prepare maintain maintain records interpretation ensuring compliance ongoing proactive mindset continuous learning growth honesty transparency resolution issues values enforcement make resolve always honestly transparent upholding integrity safety reliability high-quality reliable products beneficial society contributing skillful trained trusting deliver value returning accountable system contributes real outcomes benefits excelling customers Required Skills & Qualifications: h6id='skills'>Skills Required Include Strong Problem-Solving Approaches:& ewline Systematic Results-Oriented Experience Proven Analytical Good Time Management Effective Technical Regulatory Documentation Relevant Industry Knowledge Ability To Interpret Complex Information Design And Implement Quality Improvement Projects Planning Establishing Processes Policies Efficient Communication Team Player Leadership Advise Help Drive Compliance Enhanced Systems Streamline Process