Onsite Validation Engineer – Medical Devices (PR)

EQVAL Group, Inc; Ponce (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. seeks a Validation Engineer/Specialist to support validation activities in a Medical Devices or Pharmaceutical manufacturing environment in Puerto Rico. A Bachelor’s degree in Engineering and hands-on experience with validation documentation and protocols are required.

You will apply MSA methods, GR&R, DOEs, and use Minitab to analyze data, while delivering clear technical writing. Proficiency in English and Spanish is essential, along with strong communication.

Qualifications

• Bachelor’s degree in engineering required.
• Experience developing and executing validation documentation and protocols (URS/FRS, IQ/OQ/PQ, reports).
• Experience in Measurement System Analysis (MSA) including GR&R and DOEs.
• Strong technical writing skills and ability to communicate in English and Spanish.

Responsibilities

• Support Validation/Qualification activities in a Medical Devices or Pharmaceutical manufacturing environment.

Skills

Validation documentation

MSA/GR&R/DOEs

Minitab

Technical writing

Bilingual English/Spanish

Communication skills

Education

Bachelor's degree in Engineering

Tools

Minitab

Job description

EQVAL Group, Inc. seeks a Validation Engineer/Specialist to support validation activities in a Medical Devices or Pharmaceutical manufacturing environment in Puerto Rico. A Bachelor’s degree in Engineering and hands-on experience with validation documentation and protocols are required.

You will apply MSA methods, GR&R, DOEs, and use Minitab to analyze data, while delivering clear technical writing. Proficiency in English and Spanish is essential, along with strong communication.