Validation Scientist
QRC Group, LLC•Aibonito, PR
About The Position
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.
- Experience developing and executing validation reports.
- Experience developing and executing SOPs (Standard Operating Procedures).
- Experience with statistical data analysis.
- Ability to work on multidisciplinary projects and comply with regulatory requirements.
- Bilingual (English and Spanish).
Responsibilities
- Developing and executing validation protocols.
- Developing and executing validation reports.
- Developing and executing SOPs (Standard Operating Procedures).
- Performing statistical data analysis.
- Working on multidisciplinary projects and complying with regulatory requirements.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
No Education Listed
