Sr Analyst, QA Assurance

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Overview

This is where you make a difference in our patients’ safety. As a member of the Baxter Quality team, you will play an essential part in our mission of saving and sustaining lives. Quality is important throughout the entire product lifecycle and works collaboratively with all areas of the organization. Because Quality touches everything Baxter does, a role in Quality provides many opportunities for growth, learning and a successful career that has a daily impact on people’s lives.

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Success Profile

What makes a successful Quality team member at Baxter? Take a look at some of the top traits we’re looking for and see if you’re a fit.

Detail Oriented
Continuous Learner
Courageous
Collaborative
Critical Thinker
Influential

Sr Analyst, QA Assurance

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This is where you save and sustain lives

At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.

Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare.

Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work.

Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission.

Principais Responsabilidades:

- Acompanhar as operações de manufatura, garantindo o cumprimento dos procedimentos operacionais e requisitos de qualidade;

- Dar suporte a operação, sanando dúvidas e orientando sobre as melhores práticas a serem seguidas para garantir a qualidade dos produtos e processos;

- Conferir os documentos que envolvem a produção do lote (documentação física e/ou eletrônica de processo, sistema de controle em processo, registros de esterilização, log books das áreas, dentro outros) para liberação de lotes;

- Ser responsável pelo controle estatístico de processos (CEP), revisando os resultados periodicamente e executando os cálculos de limite, quando aplicável, usando ferramentas estatísticas (ex: minitab);

- Participar das investigações de não conformidades das áreas de manufatura assegurando o emprego de ferramentas de resolução de problemas, correta documentação e suporte no estabelecimento do plano de ação condizente com a causa raiz definida;

- Análise crítica da prática versus procedimentos/políticas e legislações aplicáveis;

- Realizar gap analysis de alterações/emissões de novas legislações ou políticas corporativas e executar as ações resultantes dessa avaliação;

- Desenvolver indicadores de performance para a área de qualidade para operações e endereçar ações para resolução dos principais problemas;

- Realizar avaliação de impacto em controles de mudança relacionados aos processos de manufatura;

- Dar treinamentos ao time operacional, encarregados e analistas referente aos processos de qualidade com interface na produção, tais como bloqueio e identificação de material/produto sob investigação, processo de retrabalho, preenchimento de documentação técnica seguindo as normas de Boas Práticas de Documentação, execução de controles em processo e tratativas para falhas, planos de amostragem e critérios de aceitação, dentre outros;

- Participar do comitê de liberação de lotes, assegurando a correta segregação e identificação do material/produto quando houver investigação e acompanhando até a conclusão dos processos;

- Realizar auditorias permanentes nas áreas produtivas, verificando o cumprimento dos procedimentos e normas, estabelecer plano de ação junto as áreas e acompanhar a conclusão deles;

- Participar de projetos de manufatura e qualidade, avaliando os impactos nas legislações e políticas corporativas, assim como nos procedimentos locais, e atuar na execução das ações de responsabilidade da área de qualidade.

Habilidades Requeridas:
• Inglês Intermediário

• Formação Superior completa em Farmácia

• Vasta experiência na área e atividades

Habilidades Desejáveis:
• Espanhol Básico

Local de trabalho: São Paulo/Zona Sul - Interlagos

Horário de trabalho - Terceiro Turno (22h - 06h) - Escala 5x2 (folgas aos Domingos e Segundas-feiras)

Equal Employment Opportunity

Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.

Reasonable Accommodations

Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information.

Recruitment Fraud Notice

Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.

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Address

Explore this location Avenida Engenheiro Eusébio Stevaux 2555
Sao Paulo- SP
04696000
Brazil Explore This Location

Hear from Our Employees

Our company is enriched by a diverse population of individuals in more than 100 countries that work to solve, innovate, manufacture and drive better healthcare options for patients around the world.

Meet Christelle, Senior Quality Manager in Malta

“I was an Engineering Graduate with a Master's in Business Administration, and was more inclined toward working with people than with machines. When I came across an opportunity to work with Baxter as a Quality Engineer, it was the perfect combination: a manufacturing environment and a role that required me to collaborate with multiple teams daily. Baxter's mission of saving and sustaining lives gives me all the purpose and fulfilment I need.”

Meet Lorena, Senior QA Associate in London, UK

“I am registered pharmacist in the UK with experience with drug products and final product release. I am very dedicated to my work and accurate in details to ensure correct assessment is provided to our customers to ensure patients' safety.”

Meet Gary, Quality Research Manager in Singapore

“I have always enjoyed working at Baxter and I find here to be a great place to work! Management truly cares for you, and invests time and resources to support your career goals and aspirations. My current role provides me the opportunity to work with culturally diverse teams, bringing different talents together, learning from one another and working toward a common goal and mission.”

Join Our Talent Community

We're grateful for your interest in a career with Baxter, and would like to get to know you. Joining our Talent Community is a great way to stay connected, learn more about Baxter, and help our recruiters find you if there's an opportunity that aligns with your background, skills and interests.

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Sr Analyst, QA Assurance

Overview

Success Profile

Sr Analyst, QA Assurance

Address

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Hear from Our Employees

Meet Christelle, Senior Quality Manager in Malta

Meet Lorena, Senior QA Associate in London, UK

Meet Gary, Quality Research Manager in Singapore

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Join Our Talent Community