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QRC Group

Validation Specialist

Aibonito, PRPresencialContratoTiempo completo

Publicado 11 sept 2026

We are looking for a qualified 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 3 to 5 years of experience in a GMP environment preferably in the pharmaceutical industry
  • Ability to work on multidisciplinary projects and comply with regulatory requirements.
  • Bilingual (English and Spanish)



Resumen del puesto

Tipo de empleo

Tiempo completo

Habilidades requeridas

Aseptic processesRegulated processesValidation protocol developmentValidation executionValidation report preparationSOP development and writingStatistical data analysisGood Manufacturing Practices (GMP) compliancePharmaceutical industry experienceMultidisciplinary/cross-functional collaborationRegulatory compliance knowledgeBilingual English-Spanish proficiencyTechnical writing (protocols, reports, SOPs)

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