Quality Engineer

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 Quality Engineer must have experience within the Pharmaceutical and/or Medical Devices manufacturing environments.
Minimum Requirements: Bachelor Degree in an Engineering or Science Field 2+ years of knowledge and experience in cGMP in a Pharmaceutical or Medical Devices manufacturing environment.
2+ years of qualification / validation protocols (IQ, OQ, PQ) development, execution and auditing for NPI projects.
Proven Knowledge in pFMEA design and analysis, CAPA investigations and analysis Knowledge on statistical analysis (GR&R) and data management (including the usage of statistical tools, i.e, Minitab).
Project management skills required.
Fully bilingual (English and Spanish).
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