Get more replies from employers
Send a job-specific resume in minutes.
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.
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.
The Validation Engineer/Specialist is required to support Validation/Qualification activities in a Medical Devices or Pharmaceutical manufacturing environment.
*This position will be full-time 100% on site in 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.
EQVAL Group is an EEO. We comply with all federal, local, and state laws regarding non-discrimination.