Process Validation Engineer

Eqval • Dorado, PR

2d • Onsite

About The Position

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 Process Validation Engineer will support operations in a Medical Devices manufacturing environment and is expected to perform the following activities and demonstrate the following qualifications:

Requirements

• Bachelor’s degree in Engineering.
• At least one (1) year of experience in Medical Device process and GMP-regulated environments (co-ops and internships are considered as experience).
• Experience in the design and execution of validation protocols and documentation, including URS, DS, IQ, OQ, and PQ, as well as deviation handling and report generation.
• Knowledge of statistical analysis (e.g., GR&R) and data management, including the use of statistical tools such as Minitab.
• Fully bilingual in English and Spanish.
• Please note that this position and requires 100% on-site presence in Dorado, Puerto Rico.

Nice To Haves

• GAP 3.0 or higher preferred.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level