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. To support our talent team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards.  We are committed to creating an environment where every team member feels included, respected, empowered and recognised.

What You Can Expect

The Quality Analyst assume the technical responsibility of the company before the respective Regional Council and the health surveillance bodies, under the terms of the legislation in force, being under its responsibility the performance and coordination of all the technical-scientific services of the company, also respecting the recommendations of the labor legislation or labor agreement

How You'll Create Impact Actively monitor and support distributors to assess the performance of quality processes and systems, identifying opportunities for improvement.Receive complaints from Zimmer Biomet products where the product failed to meet the customer expectations and follow up communication to manufacturers.Standardize and ensure compliance with procedures related to technovigilance, in line with the company's quality system.Monitor and provide support in the execution of field actions in Brazil.Manage and support quality system processes including supplier management, audits, as well as corrective and preventive actions (CAPA).Be responsible for attending local audits (such as INMETRO, Health Surveillance and the like), as well as external / corporate audits.Maintains criteria for evaluating products and suppliers in accordance with the requirements of the RDC 665/22 standard.It establishes, maintains, promotes and controls the identification of products upon receipt before they are stored and segregated.She/He must perform the functions in fact and in law, as he/she is responsible for the quality of the product and services provided as well as by information security. Disseminates and trains the other employees of the company the standards and requirements of the quality and integrity systemWhat Makes You Stand Out Strong writing, communication, and interpersonal skillsStrong attention to detail; ability to multi-task and balance competing priorities.Knowledge of overall business environment, the orthopedic industry, and the marketplaceAbility to building relationships between Quality Assurance and other areas of the organization; ability to communicate effectively at all levels.Ability to take action to solve problems, having a realistic understanding of issues (decision making and problem solving).Dealing with unresolved situations, frequent changes, delays, or unexpected events (Ambiguity Tolerance).Must possess a collaborative style to work effectively across the organization. Ability to work with people in a way that builds a high moral commitment.Strong problem-solving skills.Your Background Required English Language Level: IntermediateERP and level of knowledge: Intermediate (SAP, Protheus)Specialization Courses (if applicable): Basic computer skills, including Microsoft Office SuiteYears of experience in similar positions: 3 years minimum.Areas of expertise:  Regulatory affairs, Quality or related fields.Experience Industry: 1 year minimum in orthopedic or medical device industry preferred.Travel Expectations

EOE/M/F/Vet/Disability