Process Engineer

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. 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.

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).
• Bachelor Degree in Engineering (Electrical and Mechanical backgrounds preferred).
• Previous 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).
• Life Insurance
• Paid time off (PTO)
• Holidays
• Professional Growth (Courses and Certifications by EQVAL Academy)
• Referral program
• Productivity incentive

*This position will be full-time 100% on site in Puerto Rico.

We offer competitive compensation, benefits, and opportunities for career growth. If you are a motivated individual with passion, we would love to hear from you.

EQVAL Group is an EEO. We comply with all federal, local, and state laws regarding non-discrimination.