Equipment Validation Specialist

Pinnaql, Inc.; Humacao (PR); On-site; USD 65,000 - 90,000; Full time

Job summary

Validation & Engineering Group, Inc. seeks a dedicated Equipment Validation Specialist to lead hands-on IQ/OQ/PQ execution and qualification activities.

The role requires performing risk assessments and supporting change controls, plus assisting in commissioning and handover to operations. Ideal candidates hold a Bachelor’s in Engineering or related science and have 2–5 years in equipment validation, preferably with medical devices.

Qualifications

• Bachelor’s degree in Engineering, or related science.
• 2–5 years in equipment validation or qualification (medical devices preferred).
• Familiarity with GxP/GMP requirements and FDA expectations.
• Experience with IQ/OQ/PQ protocols and execution.
• Strong SOP and protocol writing skills; ability to produce traceable, audit-ready records.
• Communication: Bilingual (English/Spanish).
• Full-time on-site; flexible to work occasional weekends or extra hours as needed.

Responsibilities

• Hands-on execution of installation, operational and performance qualification activities.
• Perform equipment risk assessments and support change control activities.
• Support equipment commissioning and handover to operations.

Skills

Bilingual English/Spanish

Education

Bachelor’s degree in Engineering or related science

Job description

Current job opportunities are posted here as they become available.

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

• Equipment Validation Specialist

Description

• Responsible for hands‑on execution of installation, operational and performance qualification activities
• Perform equipment risk assessments and support change control activities
• Support equipment commissioning and handover to operations

Qualifications

• Bachelor’s degree in Engineering, or related science
• 2–5 years in equipment validation or qualification (medical devices preferred)
• Familiarity with GxP/GMP requirements and FDA expectations
• Experience with IQ/OQ/PQ protocols and execution
• Strong SOP and protocol writing skills; ability to produce traceable, audit‑ready records
• Communication: Bilingual (English/Spanish) — able to interact with site teams and suppliers
• Full‑time on‑site; flexible to work occasional weekends or extra hours as needed

At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose‑driven, supportive team.

Excited to build something meaningful together? We look forward to hearing from you.

Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.