Pablo Reyes

Pablo Reyes

Senior Validation Specialist @ Bristol Myers Squibb

About Pablo Reyes

Current Position at Bristol Myers Squibb

Pablo Reyes is currently a Senior Validation Specialist at Bristol Myers Squibb, based in Manatí, Puerto Rico. In this role, he leverages his extensive experience in the pharmaceutical industry to ensure compliance and effectiveness in validation processes. His position involves managing validation activities, contributing to quality assurance, and supporting corporate inspections and remediation activities.

Professional Experience at ProPharma Group

From 2016 to 2017, Pablo Reyes worked as an Independent Consultant for ProPharma Group in Hillsboro, Oregon. His role for the two-month period involved providing expert insights and validation services, highlighting his flexibility and capability to deliver on short-term, high-stakes projects within the pharmaceutical sector.

Role at Gintegra Consulting Services LLC

Pablo Reyes served as an Independent Consultant for Gintegra Consulting Services LLC from 2016 to 2017, working across multiple locations including Chiplun, India, Puerto Rico, Philadelphia, and OSS, Netherlands. Over an eight-month period, he executed and developed product transfer and special projects, demonstrating his ability to adapt and perform in diverse settings while contributing significantly to validation and quality assurance efforts.

Educational Background in Chemical Engineering

Pablo Reyes holds a Bachelor of Science (B.S.) degree in Chemical Engineering from Recinto Universitario Mayaguez, where he studied from 1977 to 1982. This solid educational foundation has been pivotal in his career, providing the technical knowledge and problem-solving skills essential for his various roles in the pharmaceutical industry.

Decade-Long Tenure at Amgen

From 2004 to 2014, Pablo Reyes worked as a Senior Validation Scientist at Amgen in Juncos, Puerto Rico. During his ten-year tenure, he managed significant validation projects, ensuring compliance with industry standards and regulatory requirements. His long service at Amgen underscores his expertise and reliability in the field of validation and quality assurance.

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