Validation Specialist
Jornada completa
QRC Group, LLC
We are looking for a qualified 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
Requirements
- 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)
Vacante publicada el 23 días atrás
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