Validation & Engineering Group
MF01-091825 Process Engineer / Qualification
Validation & Engineering Group, De Pere, Wisconsin, United States
Overview
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: Process Engineer
Experience in Process Engineering for the Medical Device Industry Experience in Qualifications
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. Strong knowledge in regulatory guidance Experience with Process Engineering and the development and execution of Validation Protocols Technical Writing skills and investigations processes. Available to work extended hours, possibility of weekends and holidays.
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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: Process Engineer
Experience in Process Engineering for the Medical Device Industry Experience in Qualifications
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. Strong knowledge in regulatory guidance Experience with Process Engineering and the development and execution of Validation Protocols Technical Writing skills and investigations processes. Available to work extended hours, possibility of weekends and holidays.
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