Process Engineer

EQVAL; Arecibo (PR); On-site; USD 75,000 - 105,000; Full time

Benefits offered by this job

Health insurance

Life Insurance

Paid time off (PTO)

Holidays

Professional Growth (EQVAL Academy)

Referral program

Productivity incentive

Job summary

EQVAL Group, Inc. seeks Process Engineers to support development, validation, and implementation of new manufacturing processes in a regulated setting.

You will generate IQ/OQ/PQ documentation and Master Validation Plans, and help design in-process inspection systems for new components. Responsibilities include DOE, PFMEA, risk analysis, and cross-functional collaboration on technologies like laser welding, injection molding, and vision systems.

Qualifications

• Bachelor degree in engineering with electrical or mechanical backgrounds.
• 4+ years in regulated pharma, biotech or medical devices.
• Experience with automated manufacturing systems and equipment.
• Automation/controls, tooling, fixtures, test method development.
• Proficiency with DOE, FMEA, CAPA and root-cause investigation.
• Strong technical writing and bilingual English/Spanish.

Responsibilities

• Support development, validation, and implementation of new manufacturing processes.
• Generate documentation including IQ/OQ/PQ reports and Master Validation Plans.
• Design in-process and receiving inspection systems for new components.
• Characterize and optimize manufacturing processes using DOE, PFMEA and risk analysis.
• Collaborate cross-functionally with teams and technologies (laser welding, molding, vision).

Skills

Process validation

Equipment qualification

DOE

FMEA

CAPA

Root-cause investigation

Technical writing

Bilingual English/Spanish

Education

Bachelor Degree in Engineering

Tools

Automated manufacturing systems

Laser welding

Heat bonding

Injection molding

Vision systems

PLC/Servo/Pneumatics/Sensors

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 support the development, validation, and implementation of new manufacturing processes. The role involves documentation generation, process optimization, and cross-functional collaboration.

Responsibilities:

• Perform process validationandequipment 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 componentsand processes.
• Characterize, optimize, and improvemanufacturing processes throughDOE, PFMEA, and risk analysis.
• Work with technologies such as laser welding, heat bonding, injection molding, vision systems, and automation (PLC/servo/pneumatics/sensors).

Key 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 manufacturingsystem and equipment (laser welding, heat bonding, injection molding, visionsystems).
• 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).

Benefits:

• Health insurance (Medical, Dental, Vision, Pharmacy)
• 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 Dorado, Puerto Rico.

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