Quality Management Systems Sr Specialist, CAPA-Medical Devices Join to apply for the Quality Management Systems Sr Specialist, CAPA-Medical Devices role at Zimmer Biomet . At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient’s mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds. As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. We focus on development opportunities, employee resource groups, flexible working environments, competitive rewards, wellness incentives, and a culture of recognition and performance awards. We are committed to an inclusive environment where every team member feels respected, empowered, and recognized. Responsibilities Facilitate CAPA investigations to resolve quality issues, including planning, execution, and verification of effectiveness. Ensure thorough documentation of CAPA procedures and audit readiness. Collaborate effectively with departments, suppliers, and external experts to meet Zimmer Quality goals. Impact Creation Coach and facilitate CAPA investigations from initiation to verification. Assist with risk analysis and containment actions. Review CAPA files for completeness and audit readiness. Qualifications Proven experience in CAPA within the Medical Devices industry, minimum 5 years. Bachelor’s degree in engineering or related field. Strong knowledge of ISO 13485 and quality standards. Excellent interpersonal, communication, and technical writing skills. English proficiency at C1 level. Certifications like CQE or CRE are a plus. Additional Information Travel may be required. We are an equal opportunity employer. Please ensure your resume is in English. #J-18808-Ljbffr