On-Site Validation Engineer – Pharma/Med Devices

EQVAL; Dorado (PR); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Health insurance (Medical, Dental, Vis

Life Insurance

PTO

Holidays

Professional Growth (EQVAL Academy)

Referral program

Productivity incentive

Job summary

EQVAL Group, Inc. seeks Validation Engineers to support development, validation and implementation of new manufacturing processes in regulated environments. The role emphasizes documentation, process optimization, and cross‑functional collaboration.

You will validate processes and equipment, develop Master Validation Plans, and work with laser welding, vision systems, and automation to ensure quality across Pharma, Biotech and Medical Devices.

Qualifications

• Bachelor degree in Engineering; Electrical or Mechanical preferred.
• Experience in regulated pharma/biotech/medical devices.
• Experience with automated manufacturing systems and equipment.
• Proficiency in DOE, FMEA, CAPA, and root‑cause investigation.
• Excellent technical writing skills; bilingual English/Spanish.

Responsibilities

• Perform process validation and equipment qualification activities (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.

Skills

DOE

FMEA

CAPA

Root-cause analysis

Bilingual English/Spanish

Education

Bachelor’s degree in Engineering

Tools

Laser welding equipment

Vision systems

PLC/servo/pneumatics

Job description

EQVAL Group, Inc. seeks Validation Engineers to support development, validation and implementation of new manufacturing processes in regulated environments. The role emphasizes documentation, process optimization, and cross‑functional collaboration.

You will validate processes and equipment, develop Master Validation Plans, and work with laser welding, vision systems, and automation to ensure quality across Pharma, Biotech and Medical Devices.