Validation & Engineering Group, Inc.
MF01-080824 QA Lab Equipment Qualification Scientist
Validation & Engineering Group, Inc., Carolina, Carolina, us, 00985
MF01-080824 QA Lab Equipment Qualification Scientist
3 weeks ago Be among the first 25 applicants 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: Responsibilities
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. Seniority level
Mid-Senior level Employment type
Contract Job function
Strategy/Planning and Information Technology Referrals increase your chances of interviewing at Validation & Engineering Group, Inc. by 2x
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3 weeks ago Be among the first 25 applicants 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: Responsibilities
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. Seniority level
Mid-Senior level Employment type
Contract Job function
Strategy/Planning and Information Technology Referrals increase your chances of interviewing at Validation & Engineering Group, Inc. by 2x
#J-18808-Ljbffr