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Veeva Vault QMS_3-6 yrs_BLR_Ami_Perm

3.00 to 6.00 Years   Bangalore   07 Mar, 2022
Arminus
Job LocationBangalore
EducationNot Mentioned
SalaryNot Disclosed
IndustryIT - Software
Functional AreaGeneral / Other Software
EmploymentTypeFull-time

Job Description

    Minimum of 3-6 years of IT experience. * Minimum of bachelor s Degree or applicable experience within information/Computer systems with focus on Qualification of R&D applications * Must have Veeva Vault skillset Having Veeva Vault QMS experience will be preferred. * Deep knowledge of Veeva Vault configuration, developing them in live projects based on client requirement. * Working knowledge of Document and Object record migration from legacy application to Veeva Vault. * Good technical knowledge in core technologies and platforms such as Java, .Net, XML, HTML, PL/SQL & API. * Previous experience in the biotechnology / Pharmaceutical / Life Science or related industry implementing and validating computer systems that manage regulated information * Working knowledge of IT infrastructure qualification processes and IT operating procedures * Solid understanding & experience in GxP, GAMP and delivering validated applications (21 CFR Part 11) * Thoroughly familiar with Quality & GxP IT compliance requirements. * Strong planning and analytical skills combined with ability to work with geographically distributed teams in a rapid development model. * Awareness of ITIL and Support Project Methodology. Key Skills: Minimum of 3-6 years of IT experience. * Minimum of bachelor s Degree or applicable experience within information/Computer systems with focus on Qualification of R&D applications * Must have Veeva Vault skillset Having Veeva Vault QMS experience will be preferred. * Deep knowledge of Veeva Vault configuration, developing them in live projects based on client requirement. * Working knowledge of Document and Object record migration from legacy application to Veeva Vault. * Good technical knowledge in core technologies and platforms such as Java, .Net, XML, HTML, PL/SQL & API. * Previous experience in the biotechnology / Pharmaceutical / Life Science or related industry implementing and validating computer systems that manage regulated information * Working knowledge of IT infrastructure qualification processes and IT operating procedures * Solid understanding & experience in GxP, GAMP and delivering validated applications (21 CFR Part 11) * Thoroughly familiar with Quality & GxP IT compliance requirements. * Strong planning and analytical skills combined with ability to work with geographically distributed teams in a rapid development model. * Awareness of ITIL and Support Project Methodology.,

Keyskills :
it complianceit infrastructureanalytical skillsdistributed teamsxmlqmsgxpcfrjavanetitilhtmlgampveevavaultplsqlscienceplanning

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