Validation Specialist

Pharma-Bio Serv, a global consulting firm headquartered in Puerto Rico, has been dedicated exclusively to providing services to the largest biotechnology & bio-engineering companies within the regulated industry for more than 25 years. Since our inception, our services have resulted in a project experience level and personnel resource base ranking among the highest worldwide.
Currently, our clients are looking to hireValidation Engineers/ Specialistto provide services in theWest Region of P.R.
The Validation Engineer will be responsible for the development of validation master plans, installation, operational and performance qualification protocols, process flow diagrams, test cases, and standard operating procedures for new or modified utilities and facilities supporting manufacturing processes, systems, or equipment. Also, the selected resource will prepare detailed reports or design statements based on results of validation, qualification and/or commissioning tests or reviews of procedures and protocols.
Minimum requirements:
Bachelor’s degree in a relevant field is required.
Minimum 1-2 years’ experience in a medical device or pharmaceutical environment performing validation activities.
Experience with Installation, Operation, and Performance validation documentation processes.Computer System Validation (CSV) experience is preferred.
Experience in documentation of technical/scientific reports/studies and risk assessments for product and process.
Preferred experience in process improvement/ process optimization.

Job Types: Full-time, Temporary
Experience:
Validation: 1 year (Required)

Education:
Bachelor's (Required)