QG
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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