Quality Engineer | Medical Devices | Temp

Support day-to-day manufacturing operations as a key quality representative on the production line. | Serve as the primary Quality Assurance representative supporting assigned manufacturing line operations. | Support validation activities, including IQ, OQ, PQ, engineering studies, protocols, reports, and qualification documentation. | Develop, review, and support product quality plans, quality specifications, risk analyses, FMEAs, and related quality system documentation.
Requisitos:
Bachelor's degree in Engineering required. | Minimum of 2 years of relevant experience in Quality and/or Compliance, preferably in the medical device industry. | Experience working with validations in medical devices or pharmaceutical environments. | Fully bilingual in English and Spanish.