A leading technical support firm in Puerto Rico seeks a Validation Specialist to review and audit validation and verification activities in pharmaceutical manufacturing. The role requires a Bachelor's or Master's degree in Chemical Engineering or a related field, along with proven experience in compliance with cGMP regulations. Strong analytical and communication skills are essential, along with bilingual proficiency in English and Spanish. This position offers a dynamic work environment focusing on regulatory impact assessments and product quality improvements. #J-18808-Ljbffr