Validation & Engineering Group
MF01-090525 Validation Engineer/Specialist
Validation & Engineering Group, De Pere, Wisconsin, United States
Job Description
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: Validation Engineer / Specialist Qualifications: Bachelor's Degree in Science or Engineering. Minimum of 2 years of experience in direct pharmaceutical, medical device or biotechnology industries. Experience in direct process / manufacturing areas. Fully bilingual (English / Spanish) with excellent oral skills. Must be proficient using MS Windows and Microsoft Office applications. Knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance. Experience in Commissioning, Qualification and Validation (CQV), Computer System Validation (CSV), URS, VP, TMX. Technical Writing skills and investigations processes. Available to work extended hours, possibility of weekends and holidays.
#J-18808-Ljbffr
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: Validation Engineer / Specialist Qualifications: Bachelor's Degree in Science or Engineering. Minimum of 2 years of experience in direct pharmaceutical, medical device or biotechnology industries. Experience in direct process / manufacturing areas. Fully bilingual (English / Spanish) with excellent oral skills. Must be proficient using MS Windows and Microsoft Office applications. Knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance. Experience in Commissioning, Qualification and Validation (CQV), Computer System Validation (CSV), URS, VP, TMX. Technical Writing skills and investigations processes. Available to work extended hours, possibility of weekends and holidays.
#J-18808-Ljbffr