Quality Engineer

hace 2 semanas


Bogotá, Colombia Zimmer Biomet A tiempo completo

Join to apply for the Quality Engineer 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, and support a culture of recognition, performance awards, and inclusion. What You Can Expect Responsible for ensuring conformity and standardization of practices for Monthly Complaint Trending Reviews (MCTRs), Quality System Trending Reviews (QSTRs) and Management Reviews (MRs) across all assigned ZB Sites. Provide crucial support in the development and ongoing management of meeting reports, assist with information gathering, report creation, and formal presentation, and ensure traceability of action items and compliance with global and site procedures. Drive process compliance, apply consistent practices across sites, and interact with various QMS functions to achieve Zimmer Biomet Quality Goals. How You'll Create Impact Development and implementation of corrective/preventative action plans and issue evaluation plans. Management of MCTRs, including processing meeting minutes/reports into the EtQ system, assigning triggers, and monitoring task completion. Management of QSTRs and MRs, including monitoring and follow-up of open action items, scheduling meetings, processing minutes/reports, and tracking task completion. Active communication with QMS functions. Maintenance of Quality Trending procedures for all assigned ZB Sites. What Makes You Stand Out Excellent oral and written communication and interpersonal skills. Proficiency in Microsoft Office Suite. Team orientation and ability to build cross‑department relationships. Results orientation and ability to meet deadlines. High potential for future development opportunities. Knowledge of ISO 13485:2016 and ISO 9001:2015. Desirable: proficiency in EtQ, SharePoint, and intermediate‑to‑advanced skills in Excel, Word, and PowerPoint, and rapid learning of new systems. Your Background A bachelor’s degree in engineering or related program with certification as a quality engineer (e.g., CQE). Certified Quality Engineer (CQE) and medical device experience, particularly in the orthopedic industry, preferred. 2‑5 years of medical device experience required, preferably in positions related to Quality Management System, CAPA processing, and management of KPIs and indicators for quality functions. Based in Bogotá. Travel Expectations Minimal travel required. Equal Opportunity EOE/M/F/Vet/Disability. Seniority Level Mid‑Senior level. Employment Type Full‑time. Job Function Quality Assurance Industries Medical Equipment Manufacturing #J-18808-Ljbffr


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