Process Validation 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 Validation Engineer must have experience with validation projects in Pharmaceutical environment. Minimum Requirements: Bachelor Degree in an Engineering or Natural Sciences field 5+ years of knowledge and experience in cGMP in a Pharmaceutical manufacturing environment. 5+ years of Design Documentation (URS, DS), IQ, OQ, PQ protocols development and execution, deviations and reports generation. 5+ years of statistical analysis (GR&R) and data management (including the usage of statistical tools, i.e, Minitab). Knowledge in Computer System Validation (CSV). Good technical writing skills in English and Spanish. Project management skills required. Fully bilingual (English and Spanish). Job Type: Full-time 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 setting: In-person Powered by JazzHR