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Analista de Processos Jr.

Req #: JR - 085636 Location São Paulo, São Paulo, Brazil Job Category: Quality Control Date Posted: 11/24/2022

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 Health &
    Well-Being Benefits

  • Paid Time Off

  • 2 Days a Year to Volunteer

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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

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Analista de Processos Jr.

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 atividades:

  • Revisão da documentação de produção (ordem de produção e formulários) de acordo com as boas práticas de documentação, seguindo os conceitos de Integridade de Dados e todos os demais procedimentos vigentes;
  • Criar e sustentar indicadores provenientes do processo de revisão da documentação de produção física e eletrônica (ordem de produção e formulários), que promovam a cultura de Right at the First time (Fazer certo da primeira vez);
  • Estruturar treinamentos para o time de operação para melhoria contínua do processo de encerramento da documentação de produção física e eletrônica (ordem de produção e formulários), de acordo com os indicadores provenientes do processo de revisão.
  • Garantir que os indicadores da área estejam dentro das métricas estabelecidas, como por exemplo: Cycle time de liberação de ordens, entre outros;
  • Criação, Revisão e/ou Obsolescência de procedimentos operacionais padrão e/ou documentos relacionados da área de soluções provenientes de: iniciativas de melhoria contínua, mudanças de processos/equipamentos, implantação de novos processos/equipamentos e/ou adequação à novas regulamentações locais, corporativas, regulatórias local ou externa;
  • Apoiar o time da área de soluções e/ou implementar projetos relacionados à excelência operacional/melhoria contínua, como: Kaizen’s, programa 6S, etc;
  • Garantir que as documentações dos processos produtivos (ordens de produção) em revisão sejam mantidas de forma organizada;
  • Criar Controles de Mudança de Documentos (CMD), bem como executar planos de ação relacionados à implementação da alteração;
  • Dar suporte no controle de OEE da área de soluções, identificando oportunidades que podem aumentar a eficiência da área;
  • Realizar compras de utensílios pertinentes à produção;
  • Executar outras atribuições correlatas de acordo com as necessidades da área.

Requisitos:

  • Superior completo – Farmacêutico/ Engenharia Química e Afins;
  • Conhecimentos de GMP/Boas Práticas de Documentação.
  • Conhecimentos de Integridade de Dados (Data Integrity).
  • Inglês – nível intermediário.
  • Microinformática como usuário – facilidade no manejo de sistemas computadorizados e Pacote Office.
  • Diferencial – Conhecimento em excel.

Mínimo de 1 ano de experiência na área.

Jornada de Trabalho: 8hrs (07 - 16h)

Reasonable Accommodations

Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please send an e-mail to [email protected] 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.

085636

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."

Christelle

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."

Lorena

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."

Gary

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.

Christelle

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."

Lorena

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."

Gary

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."

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