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Jr. Validation Specialist

Aibonito, Puerto RicoContractPosted Oct 5, 2026

Job 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)

Description copied from Qrcgroup's careers page. Read the full posting before you apply.

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