.. through the way we serve others with integrity and respect. We accomplish this by retaining the best people in the industry, focusing on training, and learning, and maintaining the best practice standards throughout all we do. Because relocation is often part of the process, we provide generous benefits .. ver más
EQVAL Group, Inc. is a company that provides services to the manufacturing industry ( Medical Devices, Pharmaceuticals, Biotechnologies, others ). We work with an extraordinary group of professionals ( employees and contractors ) to accomplish the requirements established by our customers, in order to perform and provide a highly effective service. We are looking for a Validation Specialist with Medical Devices manufacturing experience preferred (3+ years). Must possess experience in Chemical Laboratory best practices . Essential Functions : Perform assessments on Analytical Test Methods, including drive, implement and/or support actions towards findings resolution and implementation. Development and execution of Validation Protocols for Test Methods Validation (including protocols development, execution, and data analysis). Lead and/or participate in different Cleaning Validation activities. Support Cleaning Validation activities and Test Methods execution Requirements: Knowledge in Chemical Laboratory best practices. Experience in Analytical Laboratory Test Methods analysis and execution, including 'hands-on' experience performing laboratory methods and its documentation process. Knowledge in USP Guidelines and ICH Guidelines for Stability. Knowledge in Cleaning Validation activities, including protocols development and execution. 3+ years of experience in Chemical Laboratory, including 'hands-on' experience as a Laboratory Technician. Excellent technical writing skills (both English and Spanish) BS in Chemistry preferred, or related Sciences. Only local Puerto Rico candidates will be considered . Powered by JazzHR