Analista De Controle De Qualidade Pleno

J&J FAMILY OF COMPANIES

São José dos Campos, São Paulo, Brazil
Not specified
Quality control laboratory support
Regulatory compliance with bpf/gmp and glp
Investigation of laboratory deviations
Johnson & Johnson is seeking a Quality Control Analyst in São José dos Campos, Brazil, to support laboratory activities focused on quality assurance and compliance. The ideal candidate will have a strong background in quality control within the pharmaceutical industry and will be responsible for ensuring adherence to regulatory standards and continuous improvement initiatives

Job Summary

  • The role integrates the Quality Control Laboratory team providing technical support and leading continuous improvement projects to ensure compliance with regulatory standards and global quality norms.
  • The position involves coordinating corrective and preventive actions, investigating deviations, and supporting quality events with internal and global teams to maintain traceability and alignment.
  • The candidate will generate reports on trends and quality indicators, participate actively in audits, and contribute to the maintenance and review of quality procedures and documentation.

Matching Summary

Match Score: 85

Johnson & Johnson is seeking a Quality Control Analyst in São José dos Campos, Brazil, to support laboratory activities focused on quality assurance and compliance. The ideal candidate will have a strong background in quality control within the pharmaceutical industry and will be responsible for ensuring adherence to regulatory standards and continuous improvement initiatives.

Skills & Requirements

Must-have

  • Quality control laboratory support
  • Regulatory compliance with BPF/GMP and GLP
  • Investigation of laboratory deviations
  • Data integrity and ALCOA+ principles
  • Analytical method validation and verification
  • Quality metrics and trend analysis

Nice-to-have

  • Lean Six Sigma Green Belt certification
  • Experience with microbiological quality control
  • Strong verbal and written communication
  • Project management and root cause analysis
  • Collaborative and continuous improvement focus
  • Training delivery on quality tools

Key Requirements

  • Bachelor's degree in Pharmacy, Chemistry, or Chemical Engineering
  • Minimum 5 years experience in Quality Control or Analytical Development
  • Knowledge of USP, EP, ANVISA regulations
  • Advanced English proficiency desirable
  • Lean or Lean Six Sigma Green Belt certification preferred

Work Rights

Not specified

Tailored Resume

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