Validation Engineer

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.

Knowledge in 21 CFR Part 820 regulation.

Minimum 2 years of experience in the development and execution of validation documentation and protocols, including; Validation Assessments, Validation Plans, Requirements Specifications (URS, FRS), IQ, OQ, PQ and Reports.

Good technical writing skills in English and Spanish.

Experience developing and implementing Measurement System Analysis (MSA), including; Attribute Analysis, GR&R, DOEs.

Experience in Minitab (software statistical tool).

Project management skills required.

Fully bilingual (English and Spanish).

Benefits : Employee assistance program Employee discount Health insurance Life insurance Dental insurance Paid time off Professional development assistance Referral program Vision insurance Work Location : In person Powered by JazzHR