Quality Analyst

buscojobs Brasil; São Paulo; Presencial; BRL 70.000 - 100.000; Tempo integral

Resumo da oferta

A leading medical devices company in São Paulo is seeking a Quality Analyst responsible for ensuring compliance with regulatory standards and managing quality processes. The ideal candidate will have at least 3 years of experience, strong communication skills, and knowledge of SAP. This position offers the opportunity to have a significant impact on quality and safety in the orthopedic industry.

Qualificações

• Minimum of 3 years of experience in similar positions.
• Intermediate English language proficiency required.
• Expertise in regulatory affairs, quality, or related fields.

Responsabilidades

• Monitor and support distributors to assess quality processes.
• Standardize compliance with procedures related to technovigilance.
• Attend local and external audits.
• Manage supplier quality processes and corrective actions.

Conhecimentos

Strong writing skills

Communication skills

Interpersonal skills

Attention to detail

Problem-solving skills

Ferramentas

SAP

Microsoft Office Suite

Descrição da oferta de emprego

Valued Team member: We are glad you are exploring new opportunities within Zimmer Biomet!

What You Can Expect

The Quality Analyst assumes the technical responsibility of the company before the respective Regional Council and the health surveillance bodies, under the terms of the legislation in force. They are responsible for the performance and coordination of all the technical-scientific services of the company, respecting the recommendations of labor legislation or labor agreements.

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 regarding Zimmer Biomet products where the product failed to meet customer expectations and follow up with manufacturers.
• Standardize and ensure compliance with procedures related to technovigilance, in line with the company's quality system.
• Monitor and support the execution of field actions in Brazil.
• Manage and support quality system processes including supplier management, audits, and corrective and preventive actions (CAPA).
• Attend local audits (such as INMETRO, Health Surveillance, etc.) and external/corporate audits.
• Maintain criteria for evaluating products and suppliers according to RDC 665/22 standards.
• Establish, maintain, promote, and control the identification of products upon receipt before storage and segregation.
• Perform functions in fact and law, being responsible for the quality of products and services, as well as information security. Disseminate and train employees on standards and requirements of the quality and integrity system.

What Makes You Stand Out

• Strong writing, communication, and interpersonal skills.
• Strong attention to detail; ability to multi-task and manage competing priorities.
• Knowledge of the overall business environment, the orthopedic industry, and the marketplace.
• Ability to build relationships between Quality Assurance and other organizational areas; effective communication at all levels.
• Proactive problem-solving skills and decision-making ability.
• Ability to handle unresolved situations, frequent changes, delays, or unexpected events (Ambiguity Tolerance).
• Collaborative style to work effectively across the organization, fostering high morale.
• Strong problem-solving skills.

Your Background

• Required English Language Level: Intermediate.
• ERP knowledge: Intermediate (SAP, Protheus).
• Basic computer skills, including Microsoft Office Suite.
• Minimum of 3 years of experience in similar positions.
• Expertise in regulatory affairs, quality, or related fields.
• Minimum of 1 year experience in the orthopedic or medical device industry preferred.

EOE/M/F/Vet/Disability