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QRC Group

Jr. Validation Specialist

Aibonito, PRPresencialContratoTempo integral

Publicado 5 de out. de 2026

Esta vaga foi publicada em ES

We are looking for a qualified Jr. Validation Specialist with knowledge and experience with aseptic and regulated processes and developing and executing:
  • Validation protocols.
  • Validation reports.
  • SOPs (Standard Operating Procedures).
  • Statistical data analysis


Requirements

  • Bachelor in Sciences with 2 years of experience in a GMP environment preferably in the pharmaceutical industry
  • Ability to work on multidisciplinary projects and comply with regulatory requirements.
  • Experience with aseptic and regulated processes and developing and executing: Validation protocols,Validation reports, and SOPs (Standard Operating Procedures).
  • Statistical data analysis
  • Bilingual (English and Spanish)



Resumo da função

Tipo de vaga

Tempo integral

Competências necessárias

Validation Protocol DevelopmentValidation Protocol ExecutionValidation Report AuthoringSOP Development and MaintenanceStatistical Data AnalysisAseptic Process KnowledgeGood Manufacturing Practices (GMP) KnowledgeRegulatory Compliance (Pharmaceutical Regulations)Cross-functional/Multidisciplinary CollaborationTechnical Writing and DocumentationBilingual Communication (English/Spanish)Pharmaceutical Industry Experience (GMP Environment)

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