Jr. Validation Specialist
QRC Group•Aibonito, PR
About The Position
We are looking for a qualified Jr. Validation Specialist with knowledge and experience with aseptic and regulated processes and developing and executing: Validation protocols, Validation reports, SOPs (Standard Operating Procedures), and Statistical data analysis.
Requirements
- Bachelor in Sciences with 2 years of experience in a GMP environment preferably in the pharmaceutical industry.
- Ability to work on multidisciplinary projects and comply with regulatory requirements.
- 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.
- 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.
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
