Validation Specialist

QRC Group

Posted a month ago, valid for 12 days

Competitive

Contract

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Sonic Summary

We are seeking a qualified Validation Specialist with 3 to 5 years of experience in a GMP-regulated environment.
The candidate should have experience in the pharmaceutical industry and knowledge of aseptic and regulated processes.
Responsibilities include developing and executing validation protocols, reports, and SOPs, as well as conducting statistical data analysis.
The role requires the ability to work on multidisciplinary projects while ensuring compliance with regulatory requirements.
Bilingual proficiency in English and Spanish is also required for this position.

We are looking for a qualified Validation Specialist with knowledge and experience with aseptic and regulated processes and developing and executing:

Bachelor in Sciences with 3 to 5 years of experience in a GMP environment preferably in the pharmaceutical industry
Ability to work on multidisciplinary projects and comply with regulatory requirements.
Bilingual (English and Spanish)

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