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Jr. Validation Specialist

Qrc Group · qrcgroup.com
AibonitoOn-siteEntry level2+ yrsContract
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The job in short

Pharmaceutical validation specialist for aseptic and GMP processes.

Compliance

Details

Found
30 d ago · posted 2026-10-05
Location
Aibonito, Puerto Rico

Full description

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)

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