Onsite Validation Engineer – Med Device & Pharma

EQVAL Group, Inc; Ponce (PR); On-site; USD 70,000 - 100,000; Full time

Benefits offered by this job

Life Insurance

Paid time off

Holidays

Professional Growth

Referral program

Productivity incentive

Job summary

EQVAL Group, Inc. in Puerto Rico is seeking a Validation Engineer/Specialist to support validation activities in a medical devices/pharma manufacturing setting.

This full-time on-site role requires a Bachelor's in Engineering and hands-on experience with IQ/OQ/PQ, validation plans, and reports. The ideal candidate will perform MSA studies (GR&R, DOEs) using Minitab, deliver clear technical writing, and communicate fluently in English and Spanish.

Qualifications

• Bachelor’s degree in an Engineering field.
• Experience in validation documentation (IQ/OQ/PQ) and reports.
• Experience in MSA, including GR&R and DOEs.
• Strong technical writing and bilingual in English/Spanish.

Skills

Validation Plans

GR&R/DOE

Minitab

Technical Writing

Bilingual English/Spanish

MSA

Education

Bachelor's degree in Engineering

Tools

Minitab

Job description

EQVAL Group, Inc. in Puerto Rico is seeking a Validation Engineer/Specialist to support validation activities in a medical devices/pharma manufacturing setting.

This full-time on-site role requires a Bachelor's in Engineering and hands-on experience with IQ/OQ/PQ, validation plans, and reports. The ideal candidate will perform MSA studies (GR&R, DOEs) using Minitab, deliver clear technical writing, and communicate fluently in English and Spanish.