Validation Specialist
Jornada completa
QRC Group, LLC
We are looking for a qualified Validation Specialist with experience in GMP-regulated environments and pharmaceutical processes.
Requirements
- 3 to 5 years of experience in a GMP environment.
- Experience in the pharmaceutical industry.
- Knowledge of and experience with aseptic and regulated processes.
- Experience developing and executing:
- Validation protocols.
- Validation reports.
- SOPs (Standard Operating Procedures).
- Statistical data analysis.
- Validation protocols.
- Ability to work on multidisciplinary projects and comply with regulatory requirements.
- Bilingual (English ans Spanish)
Vacante publicada el 3 días atrás
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