Aibonito, Puerto Rico | Posted on 07/27/2026
We are looking for a qualified Validation Specialist with experience in GMP-regulated environments and pharmaceutical processes.
Requirements
- 1 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.