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Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact.

• Ensure ongoing compliance of the S&R EMEA Organization to requirements originating from applicable Quality standards, regulations & policies.
• Facilitate Compliance Management reviews at prescribed intervals each fiscal year to review the continuing suitability, adequacy, and effectiveness of the S&R EMEA Organization’s Compliance strategies and programs.
• Provision of relevant information and data to S&R EMEA management, that facilitates evaluation of the adequacy and effectiveness of current compliance strategies and programs.
• Monitor compliance metrics and identify improvement opportunities.
• Collect and analyze data to identify root causes of compliance issues and performance shortfalls.
• Ensure timely and effective follow up of compliance actions (e.g. CAPA, Change Control, Regulatory actions etc.).
• Act as a Compliance SME ensuring a first-time right approach to activities affecting compliance to requirements.
• Support compliance audit and inspection preparation, resolution of audit and inspection findings and liaise with auditing groups and inspectors through all stages of the audits.
• Prepare reports and/or necessary documentation to meet requirements and ensure applicable (internal and external) stakeholders are adequately informed.
• Plan, perform, and implement process improvement initiatives to enhance compliance and operational efficiency.

• Bachelor’s degree with a minimum of 4 years of relevant experience, or a Master’s degree with a minimum of 2 years of relevant experience in Quality, Compliance, or Process Improvement
• Experience in medical device or similarly regulated industry
• Fluent written and spoken English language
• Experience in planning, coordinating, communicating, influencing, achieving milestones, resolving issues
• Ability to work in a cross functional and global environment and cultural awareness
• Good communication and interpersonal skills and ability to work independently
• Proven experience in cross-functional stakeholder management
• Project management skills
• Good presentation skills