Validation Engineer / Specialist

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. Validation Engineer/Specialist is required to support Validation/Qualification activities in a Medical Devices manufacturing environment. Minimum Requirements: Bachelor Degree in Engineering Field (Mechanical, Electrical, Industrial Engineers preferred). Knowledge in 21 CFR Part 820 regulation. Experienced (3-5 years) in the development and execution of validation documentation and protocols, including; Validation Assessments, Validation Plans, Requirements Specifications (URS, FRS), IQ, OQ, PQ and Reports. Experience developing and implementing Measurement System Analysis (MSA), including; Attribute Analysis, GR&R, DOEs. Project management skills required. Fully bilingual (English and Spanish). Experience in Minitab (software statistical tool). Good technical writing skills. Only local candidates will be considered . Powered by JazzHR