Validation Engineer
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EQVAL Group, Inc. is a company that provides technical and engineering services to the manufacturing industry (Medical Devices, Pharmaceuticals, Biotechnologies) and other service companies. We work with an extraordinary group of professionals (employees and contractors) to accomplish the requirements established by our customers, to perform and provide a highly effective service.
The Validation Engineer will support Validation/Qualification activities in a Medical Devices manufacturing environment.
Minimum Requirements:
Bachelor Degree in Engineering Field (Mechanical, Electrical, Industrial Engineers preferred).
Experienced in Medical Devices and/or Pharmaceutical manufacturing environments.
Experienced (2+ 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 in Minitab (software statistical tool).
Fully bilingual (English and Spanish).
On-site role – Applicants must currently reside in Puerto Rico
Job Types: Full-time, Contract
Work Location: In person