Validation & Engineering Group, Inc.
MF01-101624 CSV / Manufacturing Eng. Specialist
Validation & Engineering Group, Inc., Aibonito, Aibonito, us, 00705
Overview
MF01-101624 CSV / Manufacturing Eng. Specialist at Validation & Engineering Group, Inc. The company provides services for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the areas of Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services. Qualifications
Bachelor'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. About the role
The position covers CSV and Manufacturing Engineering responsibilities in a biopharma/pharmaceutical context, with emphasis on validation activities and documentation per client and regulatory requirements.
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MF01-101624 CSV / Manufacturing Eng. Specialist at Validation & Engineering Group, Inc. The company provides services for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the areas of Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services. Qualifications
Bachelor'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. About the role
The position covers CSV and Manufacturing Engineering responsibilities in a biopharma/pharmaceutical context, with emphasis on validation activities and documentation per client and regulatory requirements.
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