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QRC Group

Jr. Validation Specialist

Aibonito, PRВ офисеКонтрактПолная занятость

Опубликовано 5 окт. 2026 г.

Эта вакансия опубликована на 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)



Кратко о роли

Тип работы

Полная занятость

Требуемые навыки

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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