Validation Specialist

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.
Validation Specialist is required to support Validation/Qualification activities in a Medical Devices manufacturing environment.
Minimum Requirements: Bachelor Degree in Engineering or Science Field Minimum of 2 years experience in in the development and execution of validation documentation and protocols, including; Validation Assessments, Validation Plans, Requirements Specifications (URS, FRS), IQ, OQ, PQ and Reports. Knowledgeable of the industry standards and regulations, such as ISO, FDA, GMP, or GLP.
Experience developing and implementing Measurement System Analysis (MSA), including; Attribute Analysis, GR&R, DOEs. Project management skills required.
Fully bilingual (English and Spanish).
Experience in Minitab (software statistical tool).
Good technical writing skills.
Interact with cross functional departments to obtain validation data.
Good collaboration and interpersonal skills in order to work with various stakeholders.
Benefits: Dental insurance Employee assistance program Employee discount Health insurance Life insurance Paid time off Professional development assistance Referral program Schedule: 8 hour shift Day shift Monday to Friday Work Location: In person Powered by JazzHR