Validation Engineer

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

Benefits offered by this job

Life Insurance

PTO

Holidays

Professional Growth (EQVAL Academy)

Referral program

Productivity incentive

Job summary

EQVAL Group, Inc. is a company serving the manufacturing sector, including Medical Devices, Pharmaceuticals, and Biotech.

We seek a Validation Engineer to support development, validation, and implementation of new manufacturing processes, with emphasis on documentation, optimization, and cross-functional collaboration. The position requires a Bachelor Degree in Engineering, on-site work in Dorado, and experience in regulated industries.

Qualifications

• Bachelor Degree in Engineering (Electrical and Mechanical backgrounds preferred).
• Experience with regulated industry (Pharma, Biotech, or Medical Devices).
• Proficiency in DOE, FMEA, CAPA, and root-cause investigation.
• 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 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

DOE

FMEA

CAPA

Root cause analysis

Technical writing

Automation/controls

Education

Bachelor Degree in Engineering

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 Validation 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).

*This position will be full-time 100% on site in Dorado, 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.

• Life Insurance
• Paid time off (PTO)
• Holidays
• Professional Growth (Courses and Certifications by EQVAL Academy)
• Referral program
• Productivity incentive

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