Jr. Validation Specialist
Qrc Group · qrcgroup.com
AibonitoOn-siteEntry level2+ yrsContract
Straight from the company’s own careers site.
The job in short
Pharmaceutical validation specialist for aseptic and GMP processes.
Compliance
Details
- Found
- 30 d ago · posted 2026-10-05
- Location
- Aibonito, Puerto Rico
Full description
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).
• 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 and developing and executing: Validation protocols,Validation reports, and SOPs (Standard Operating Procedures).
• Statistical data analysis
• Bilingual (English and Spanish)