Job Description
MF Qualification / Computer System Validation (CSV) Scientist
Asegúrese de leer detenidamente la información sobre esta oportunidad antes de presentar su candidatura.
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:
Qualification / Computer System Validation (CSV) Scientist
Qualifications:
Bachelor's Degree in Science or Engineering.
Minimum of 3 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.
Strong knowledge in cGxP and regulatory guidance.
SDLC documents (i.e. URS, FDS, VP, DQ, TMX, Risk Assessment), Data Integrity, Factory Acceptance Test (FAT) & Site Acceptance Test IOPQ
Technical Writing skills and investigations processes. xugodme
Available to work extended hours, possibility of weekends and holidays.
#J-18808-Ljbffr
Asegúrese de leer detenidamente la información sobre esta oportunidad antes de presentar su candidatura.
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:
Qualification / Computer System Validation (CSV) Scientist
Qualifications:
Bachelor's Degree in Science or Engineering.
Minimum of 3 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.
Strong knowledge in cGxP and regulatory guidance.
SDLC documents (i.e. URS, FDS, VP, DQ, TMX, Risk Assessment), Data Integrity, Factory Acceptance Test (FAT) & Site Acceptance Test IOPQ
Technical Writing skills and investigations processes. xugodme
Available to work extended hours, possibility of weekends and holidays.
#J-18808-Ljbffr
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