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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.
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.