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MF01-101624 CSV / Manufacturing Eng. Specialist
Validation & Engineering Group, IncAibonito, 009Hace más de 30 días
Descripción del trabajoBachelor's Degree in Science or Engineering. Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries. Must be fully bilingual (English / Spanish) with excellent oral skills. Must be proficient using MS Windows and Microsoft Office applications. Experience in Design Documentation (URS, DS), IQ, OQ, PQ protocols development and execution, deviations and reports generation. SDLC, Risk Assessment, Data Integrity, Factory Acceptance Test (FAT) & Site Acceptance Test (SAT). Technical Writing skills and investigations processes. Available to work extended hours, possibility of weekends and holidays.
Department : Field - MF Location : Aibonito, 009
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Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas : Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.
We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position :
- CSV / Manufacturing Eng. Specialist
Qualifications :
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Specialist • Aibonito, 009