Validation & Engineering Group Inc.
QA Lab Equipment Qualification Scientist
Validation & Engineering Group Inc., Chapel Hill, North Carolina, United States, 27517
QA Lab Equipment Qualification Scientist
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: QA Lab Equipment Qualification Scientist Develop and execute qualification documents including CSV test scripts Change Control Owner Review and approve qualification documents Qualifications: Bachelor's Degree in Science or Engineering. Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries. Experience in direct process / manufacturing areas. Must be fully bilingual (English / Spanish) with excellent oral skills. Must be proficient using MS Windows and Microsoft Office applications. Experience in Computer System Development Life Cycle (SDLC) i.e. VP, URS, RA, SDS, FDS, TMX, IOPQ, Thermal Mapping (preferable) Technical Writing skills and investigations processes. Available to work extended hours, possibility of weekends and holidays.
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: QA Lab Equipment Qualification Scientist Develop and execute qualification documents including CSV test scripts Change Control Owner Review and approve qualification documents Qualifications: Bachelor's Degree in Science or Engineering. Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries. Experience in direct process / manufacturing areas. Must be fully bilingual (English / Spanish) with excellent oral skills. Must be proficient using MS Windows and Microsoft Office applications. Experience in Computer System Development Life Cycle (SDLC) i.e. VP, URS, RA, SDS, FDS, TMX, IOPQ, Thermal Mapping (preferable) Technical Writing skills and investigations processes. Available to work extended hours, possibility of weekends and holidays.