Process Engineer: Validation, Automation & Optimization

EQVAL Group, Inc; Dorado (PR); On-site; USD 65,000 - 95,000; Full time

Benefits offered by this job

Life Insurance

Paid time off

Holidays

Professional Growth (EQVAL Academy)

Referral program

Productivity incentive

Job summary

EQVAL Group, Inc. seeks a Process Engineer for full-time, on-site work in Puerto Rico. The role focuses on developing, validating, and implementing new manufacturing processes within regulated industries such as Pharma, Biotech, or Medical Devices.

You will lead DOE/FMEA-based process optimization, generate master validation plans, and work with automated systems (laser welding, vision systems). Strong technical writing and bilingual English/Spanish are required.

Qualifications

• Bachelor Degree in Engineering (Electrical or Mechanical preferred).
• Experience in regulated industries (Pharma, Biotech, Medical Devices).
• Experience with automated manufacturing systems and equipment (laser welding, vision systems).
• Proficiency in DOE, FMEA, CAPA, and root‑cause investigation.
• Fully bilingual in English and Spanish.
• Strong technical writing skills.

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).

Skills

Process engineering

DOE

FMEA

Documentation

Bilingual: English/Spanish

Education

Bachelor Degree in Engineering

Tools

Automation systems

Calibration procedures

Job description

EQVAL Group, Inc. seeks a Process Engineer for full-time, on-site work in Puerto Rico. The role focuses on developing, validating, and implementing new manufacturing processes within regulated industries such as Pharma, Biotech, or Medical Devices.

You will lead DOE/FMEA-based process optimization, generate master validation plans, and work with automated systems (laser welding, vision systems). Strong technical writing and bilingual English/Spanish are required.