I am interested to apply for a job opportunity within the Quality-Process Departments for pharmaceutical industry. I enclose my resume as a first step in exploring the possibilities of employment. I have worked as Quality Assurance - Technical Services Manager for a Medical Devices Company at Dominican Republic Operations. This recent experience included an international transfer from Puerto Rico to Dominican Republic to perform as QA Manager responsible for the Design, Validation and Implementation of scientific processes and equipment for the start-up of Laboratories, Sterilization and Final Manufacturing Processes into the new Site Operations. Commissioning, Qualification as well as their Scientific Process Validations were completed under my responsibilities as part of the validation project. As QA Manager I was also responsible for the implementation of Corporate Quality program into the new site operations, assuring the proper implementation of Compliance – CAPA program including Site Quality Key Process Standards and Regulated training program.

Highlights:

• Laboratory Management
• Scientist
• Validation
• Compliance
• Sterilization
• CAPA - Regulatory
• IQ,OQ,PQ expert
• Gurabo, P.R.