Analista De Controle De Qualidade Pleno

J&J FAMILY OF COMPANIES

São José dos Campos, São Paulo, Brazil
Not specified (assumed on-site due to the nature of the role).
Quality control laboratory support
Regulatory compliance with bpf/gmp and glp
Investigation of laboratory deviations
Johnson & Johnson is seeking a Quality Control Analyst to join their team in São José dos Campos, Brazil. The role involves providing technical support in quality assurance, implementing analytical methods, and ensuring compliance with regulatory standards in the pharmaceutical industry

Job Summary

  • The role integrates into 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 maintaining communication with external sites and global teams to ensure alignment and traceability.
  • The candidate will support analytical microbiological and physicochemical routines, participate in audits, and generate reports and dashboards to monitor quality performance and support internal reviews.

Matching Summary

Match Score: 85

Johnson & Johnson is seeking a Quality Control Analyst to join their team in São José dos Campos, Brazil. The role involves providing technical support in quality assurance, implementing analytical methods, and ensuring compliance with regulatory standards in the pharmaceutical industry.

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 implementation
  • Quality metrics and trend analysis
  • CAPA and change control management

Nice-to-have

  • Lean Six Sigma Green Belt certification
  • Experience with microbiological quality control
  • Strong verbal and written communication skills
  • Project management and root cause analysis
  • Collaborative and continuous improvement mindset
  • Experience with electronic quality systems
  • 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
  • Advanced English proficiency preferred
  • Postgraduate degree in Quality preferred
  • Experience in pharmaceutical industry quality control
  • Knowledge of USP, EP, ANVISA regulations
  • Lean Six Sigma Green Belt or equivalent certification preferred

Work Rights

Not specified

Tailored Resume

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