Estagiário - Controle de Qualidade
On-siteSão Paulo, São Paulo, Brazil
Job Summary
Conduct physical-chemical analyses on bulk and semi-finished product samples following established analytical methods and standard operating procedures. Assist in opening, tracking, and registering Out-of-Specification (OOS/RFE) and Trend (OOT/RFT) investigations alongside the Quality Control team. Ensure all activities and records comply with Good Manufacturing Practices (BPF), Good Laboratory Practices (BPL), and Good Distribution Practices (BPD) alongside applicable Anvisa regulations. Complete analytical notebooks, reports, and laboratory documentation clearly, rigorously, and traceably. Organize the laboratory, prepare reagents and solutions, and maintain analytical workflows to meet company deadlines. Requires a university degree in Pharmacy, Chemistry, or Chemical Engineering (completion expected within 1.5 years), basic knowledge of analytical techniques, and familiarity with BPF/BPL/BPD norms. Benefits include medical assistance, product discounts, and various allowances.
Required Qualifications
- Cursando Ensino Superior em Farmácia, Química, Engenharia Química ou áreas correlatas (previsão de formação a partir de 1 ano/1 ano e meio)
- Noções básicas ou de técnicas analíticas físico-químicas
- Conhecimento básico das normas de BPF, BPL e BPD
- Pacote Office básico/intermediário
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