Process Engineer

EQVAL•Arecibo, PR

20d•Onsite

About The Position

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 seeking Process Engineers that will supports the development, validation, and implementation of new manufacturing processes. The role involves documentation generation, process optimization, and cross-functional collaboration.

Requirements

Bachelor Degree in Engineering (Electrical and Mechanical backgrounds preferred).
4+ years of experience in regulated industry (Pharma, Biotech, or Medical Devices).
Experience with automated manufacturing system and equipment (laser welding, heat bonding, injection molding, vision systems).
Experience with automation/controls, tooling, fixtures, test method development.
Proficiency in DOE, FMEA, CAPA, and root‑cause investigation.
Good technical writing skills.
Fully bilingual (English and Spanish).

Responsibilities

Perform process validation and equipment qualification activities / reports (IQ, OQ, PQ) and develop Master Validation Plans.
Generate equipment documentation (evaluations, PM/calibration procedures) and manufacturing instructions.
Design and develop in‑process and receiving inspection systems for new components and processes.
Characterize, optimize, and improve manufacturing processes through DOE, PFMEA, and risk analysis.
Work with technologies such as laser welding, heat bonding, injection molding, vision systems, and automation (PLC/servo/pneumatics/sensors).