Senior Quality Analyst (Based in São Paulo)

Edwards Lifesciences Gruppe; São Paulo; Presencial; BRL 180 000 - 240 000; Tempo integral

Resumo da oferta

Edwards Lifesciences in São Paulo, Brazil, is seeking a seasoned Quality professional to support quality systems, post-market surveillance, and regulatory compliance across the product lifecycle. You will collaborate with cross-functional teams to ensure product safety, effectiveness, and continuous improvement.

The role requires 5+ years in Quality, Regulatory Affairs, or related areas within medical devices or pharmaceuticals, fluent English, and onsite work four days per week in Brazil.

Qualificações

• 5+ years of experience in Quality, Quality Systems, Post-Market Surveillance, Complaint Handling, Regulatory Affairs, or related areas.
• Experience in medical devices or pharmaceutical industries.
• Fluent English; Spanish a plus.

Responsabilidades

• Supports quality systems and regulatory compliance across product lifecycle.
• Manages field actions, CAPA and post-market surveillance investigations.
• Leads training on quality systems and process improvements.
• Prepares customer communications and collaborates with commercial teams.

Conhecimentos

Quality Systems

Regulatory Affairs

Post-Market Surveillance

Complaint Handling

Data Analysis

Cross-functional teamwork

Formação académica

Bachelor's degree in Pharmacy

Biomedical Sciences

Engineering

Life Sciences

Descrição da oferta de emprego

Imagine how your ideas and expertise can change a patient's life. Our Quality teams help shape the development of groundbreaking technologies to ensure each stage of our innovation process is held to the highest standards of integrity and safety. You'll bring your passion for problem solving and partner with various teams to influence decision-making for a product's entire lifecycle. Your work will involve you optimizing product development to impact patients around the world with pioneering technology.

How you'll make an impact Applies professional expertise and sound judgment to support quality systems, quality analysis activities, and business outcomes. Management of field actions and post-integration regulatory transitions, oversight of multi-country regulatory requirements, and cross-country coordination with senior stakeholders. Identifies, leads, and implements business process improvement initiatives for Quality Systems, including developing and enhancing procedures to improve operational efficiency, compliance, and user experience while maintaining process integrity. Provides first-level support to Quality System users, including troubleshooting issues related to CAPA and other quality systems, escalating to IT when appropriate. Leads projects from initiation through completion, including defining milestones, coordinating resources, and representing Quality on cross-functional teams. Serves as a key partner to commercial, field-based, and cross-functional teams, providing guidance and support on quality-related processes, complaint handling, and regulatory requirements. Manages post-market surveillance activities, including the receipt, documentation, investigation, trending, and reporting of customer complaints in compliance with applicable regulatory requirements. Prepares customer response communications and collaborates with commercial teams to ensure timely and appropriate follow-up on quality-related matters. Collects, analyzes, and interprets quality metrics and complaint data, identifying trends, recommending improvements, and supporting data-driven decision-making. Participates in complaint review committees and cross-functional business reviews, preparing, analyzing, and presenting quality data and trends to stakeholders. Supports field corrective actions, safety communications, recalls, alerts, and other post-market quality activities as required. Assists with internal audits, distributor audits, supplier audits, and compliance-related initiatives, ensuring adherence to quality standards and regulatory requirements. Determines training needs, develops training materials, and delivers training programs to support effective use of quality systems and processes. Recommends changes to documentation associated with Quality Systems and evaluates the effectiveness of implemented improvements.

What you will need

Bachelor's degree in pharmacy, Biomedical Sciences, Engineering, Life Sciences, or a related field. 5+ years of experience in Quality, Quality Systems, Post-Market Surveillance, Complaint Handling, Regulatory Affairs, or related areas. Experience within the medical device or pharmaceutical industries. Knowledge of quality systems, complaint management processes, and applicable regulatory requirements. Experience analyzing quality data, identifying trends, and supporting investigations and corrective actions. Fluent English required. Spanish proficiency preferred. Strategic mindset, leadership potential, and ambition to develop into a people leadership/managerial role Availability to work onsite four days per week.

What else will help you

Experience in the medical device industry is highly preferred. Knowledge of Latin American post-market regulatory requirements and reporting processes. Demonstrated ability to build strong relationships and effectively collaborate with diverse stakeholders across commercial, field, operations, and quality teams. Strong organizational skills, attention to detail, and ability to manage multiple priorities in a fast-paced environment. Hands-on mindset with a willingness to take ownership of a broad range of responsibilities. Strong analytical, critical thinking, and problem-solving capabilities.

Edwards Lifesciences is the leading global structural heart innovation company, driven by a passion to improve patient lives. Through breakthrough technologies, world-class evidence and partnerships with clinicians and healthcare stakeholders, our employees are inspired by our patient-focused culture to deliver life-changing innovations to those who need them most.