Veg Group
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Validation & Engineering Group, Inc.
(V&EG) is a leading services supplier providing solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in areas such as Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services. We are seeking a talented, dedicated individual committed to working under the highest ethical standards for the following position: Validation Specialist Qualifications: Bachelor's Degree in Engineering. Minimum of 3 years of experience in the pharmaceutical, medical device, or biotechnology industries. Experience in process / manufacturing areas. Fully bilingual in English and Spanish with excellent oral communication skills. Proficient in MS Windows and Microsoft Office applications. Strong knowledge of cGxP and regulatory guidance, with understanding of their application to regulatory compliance. Experience in designing documentation such as URS, DS, IQ, OQ, PQ protocols development and execution, deviations, and report generation. Knowledge of SDLC, Risk Assessment, Data Integrity, Factory Acceptance Test (FAT), and Site Acceptance Test (SAT). Preferred experience with medical device equipment. Technical writing skills and familiarity with investigation processes. Availability to work extended hours, including weekends and holidays.
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(V&EG) is a leading services supplier providing solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in areas such as Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services. We are seeking a talented, dedicated individual committed to working under the highest ethical standards for the following position: Validation Specialist Qualifications: Bachelor's Degree in Engineering. Minimum of 3 years of experience in the pharmaceutical, medical device, or biotechnology industries. Experience in process / manufacturing areas. Fully bilingual in English and Spanish with excellent oral communication skills. Proficient in MS Windows and Microsoft Office applications. Strong knowledge of cGxP and regulatory guidance, with understanding of their application to regulatory compliance. Experience in designing documentation such as URS, DS, IQ, OQ, PQ protocols development and execution, deviations, and report generation. Knowledge of SDLC, Risk Assessment, Data Integrity, Factory Acceptance Test (FAT), and Site Acceptance Test (SAT). Preferred experience with medical device equipment. Technical writing skills and familiarity with investigation processes. Availability to work extended hours, including weekends and holidays.
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