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QG

QRC Group

Jr. Validation Specialist

Aibonito, PRבמשרדחוזהמשרה מלאה

פורסם 5 באוק׳ 2026

המשרה פורסמה ב־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)



תצלום תפקיד

סוג משרה

משרה מלאה

כישורים נדרשים

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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