Empleos de EQVAL Group, Inc en Puerto Rico

The Buyer/Purchasing Agent will coordinate price change processes ensuring timely updates to prices payment terms and Incoterms in a Medical Device Manufacturing environment.Bachelor's degree in Business Supply Chain or related field · Minimum of 2 years of experience in purchasi ...

The Facilities Engineer will support operations in a Medical Devices manufacturing environment. · Bachelor's degree in Engineering (Mechanical, Electrical, or Industrial preferred) · 3–5 years of experience in facilities and utilities preventive maintenance programs · Experience ...

Buscamos a un/a Process Engineer para un proyecto en el Este de Puerto Rico. · ...

The Process Validation Engineer will support operations in a Medical Devices manufacturing environment. · Bachelor's degree in Engineering. · At least one (1) year of experience in Medical Device process and GMP-regulated environments. · ...

We are seeking a Quality Engineer to support projects and day-to-day manufacturing operations within a regulated environment. · Support Engineering and Quality teams in projects and day-to-day manufacturing operations · Work with Quality Systems, including the development, implem ...

We are seeking multiple Validation Engineers to support projects in Juncos, PR. · Develop and execute process validation documentation (IQ, OQ, PQ) · Develop and execute equipment qualification protocols (IQ, OQ, PQ) · ...

The Validation Engineer will support Validation/Installation activities in a Medical Devices manufacturing environment. · Good technical writing skills in English and Spanish are required. · ...

The Project Engineer will lead and coordinate engineering projects. The project engineer will be responsible for leading and coordinating engineering projects. · ...

Nos encontramos en la búsqueda de un/a Quality Specialist para un proyecto en el área Sur de Puerto Rico, dentro de la industria de Medical Devices. · ...

The Computer System Validation (CSV) Engineer will support the validation, testing, and documentation of computer systems to ensure compliance with regulatory and quality standards. · ...

The Quality Engineer will support product transfer activities from development through commercial release, · ensuring manufacturing processes and quality systems are compliant and ready to support commercial production in a regulated medical device environment.Bachelor's Degree i ...