Principal Engineer, Quality Systems

Imagine how your ideas and   expertise   can change a patient’s life. Our Global   Operations &   Quality   team plays a central part in ensuring our products are delivered to patients with cardiovascular disease.   You’ll   partner cross-functionally with manufacturing operations and sales teams, delivering thoughtful solutions to complex challenges all while developing your knowledge of the medical device industry. Whether your work includes strategic inventory planning, labeling, warehouse management, material handling, or any of our other supply chain opportunities, you will be making a meaningful contribution to our team and to patients all over the world.   Ensure compliance of the QMS and compliance within quality processes (e.g., CAPA. NCR, ECR, internal and external auditing, training). Maintain quality reporting inclusive quality and production indicators. How you'll make an impact: • Provide complex assessments including audits to ensure conformance with applicable regulations and EW policies and procedures. Assess objective evidence to determine conformity to requirements listed above, including ranking the levels of nonconformance findings • Provide technical guidance and lead projects, based on understanding of international standards and regulations, to business unit and/or corporate quality initiatives including special projects, such as designing and/or recommending systems, procedures, etc. • Plan annual audit schedule, determine and assign SMEs to audits, establish audit content, allocate time, and schedule meetings. Assess previous audit findings to establish priorities and strategies • Execute audit considering scope to assure efficient and effective use of scheduled time allocations • Identify, lead and implement business process improvement solutions for Quality Systems, including developing changes to procedures, to improve operation, efficiencies, and user experience, while supporting the integrity of the business process. Local process owner for quality system processes (e.g., CAPA, NCR, internal auditing, risk management) • Provide teams first-level support to Quality, Documentation and PCS Systems users, e.g., CAPA, NCR, Change, Training, Maintenance, for system usage and process requirements • Recommend changes to documentation associated with Quality, Documentation and PCS Systems, including assessing effectiveness and approving recommendations others • Identify continuous improvement opportunities including performing complex analysis and may present metrics to all level of the organization • Train, coach, and guide lower-level employees on more complex procedures • Other incidental duties What you'll need (Required): Bachelor's Degree in Scientific field with 6 years minimum of experience, including either industry or industry/education or Master's Degree or equivalent in Scientific field, 5 years minimum of experience, including either industry or industry/education Required or Ph.D. or equivalent in Scientific field, 2 years minimum of experience, including either industry or industry/education What else we look for (Preferred): • Proven expertise in MS Office Suite and experience with quality systems (e.g., CAPA, Ignite) • Experienced in GxP • Good project management skills and related software tools preferred • Excellent written and verbal communication skills including influencing and relationship management skills • Strong problem-solving and critical thinking skills • Ability to read, comprehend, write and speak English fluently, required • Full knowledge and understanding of Edwards policies, procedures, and guidelines relevant to quality systems • Excellent knowledge of medical or pharmaceutical regulations as relating to documentation • Excellent understanding of medical devices regulations (e.g., FDA (21 CFR Part 820) and ISO13485, ISO14971, and MDD) • Strict attention to detail • Ability to interact professionally with all