Job Description
Job Summary for Veeva Vault RIM:
Must have experience in the Veeva RIM Registrations module or at least Veeva RIM/QMS implementation experience.Responsibilities and Experience:The ideal candidate must have hands-on experience in implementing the Veeva RIM Registrations module or at least Veeva RIM/QMS implementation experience.5 to 7+ years' experience in Veeva Regulatory Information Management systems and Pharma/Biotech Drug Manufacturing Process.Analyze current state challenges with Regulatory Affairs CMC and QA (both Clinical and Commercial) business process – in the areas of planning, submission, and batch releaseIn-depth understanding of Regulatory process, for both clinical and commercial, as well as US and EU regulatory process and how it impacts the key business processes regarding initial application filings, clinical study changes, and post-marketing changes, etc.Develop a future business process for RA CMC data entry and QA batch release related to planning, submission, and batch release – in lieu of current state challenges and areas of improvementFacilitate workshops designed to define and document core business processes focusing on client's Regulatory Affairs CMC and QA future requirementsDefine future approach to implement out of the box Product Docket/ Regulatory Information Management packaged softwareHighlight and prioritize pain points across people, process, data, and technology and identify opportunities for improvement across end-to-end Regulatory, Supply Chain, and Quality business processAuthor critical deliverables within the business process workstream e.g. SIPOCs, KPIs/metrics, and Process Maps, GPID implementation roadmapHelp develop/refine Key Performance Indicators, metrics, and criteria to measure and assess RA CMC and QA operational performance
Employee Status : Full Time Employee
Shift : Day Job
Travel : No
Job Posting : Mar 1+ 2026
About Cognizant
Cognizant (Nasdaq-100: CTSH) is one of the world's leading professional services companies, transforming clients' business, operating and technology models for the digital era. Our unique industry-based, consultative approach helps clients envision, build and run more innovative and efficient businesses. Headquartered in the U.S., Cognizant is ranked 185 on the Fortune 500 and is consistently listed among the most admired companies in the world. Learn how Cognizant helps clients lead with digital at www.cognizant.com or follow us @Cognizant.
Must have experience in the Veeva RIM Registrations module or at least Veeva RIM/QMS implementation experience.Responsibilities and Experience:The ideal candidate must have hands-on experience in implementing the Veeva RIM Registrations module or at least Veeva RIM/QMS implementation experience.5 to 7+ years' experience in Veeva Regulatory Information Management systems and Pharma/Biotech Drug Manufacturing Process.Analyze current state challenges with Regulatory Affairs CMC and QA (both Clinical and Commercial) business process – in the areas of planning, submission, and batch releaseIn-depth understanding of Regulatory process, for both clinical and commercial, as well as US and EU regulatory process and how it impacts the key business processes regarding initial application filings, clinical study changes, and post-marketing changes, etc.Develop a future business process for RA CMC data entry and QA batch release related to planning, submission, and batch release – in lieu of current state challenges and areas of improvementFacilitate workshops designed to define and document core business processes focusing on client's Regulatory Affairs CMC and QA future requirementsDefine future approach to implement out of the box Product Docket/ Regulatory Information Management packaged softwareHighlight and prioritize pain points across people, process, data, and technology and identify opportunities for improvement across end-to-end Regulatory, Supply Chain, and Quality business processAuthor critical deliverables within the business process workstream e.g. SIPOCs, KPIs/metrics, and Process Maps, GPID implementation roadmapHelp develop/refine Key Performance Indicators, metrics, and criteria to measure and assess RA CMC and QA operational performance
Employee Status : Full Time Employee
Shift : Day Job
Travel : No
Job Posting : Mar 1+ 2026
About Cognizant
Cognizant (Nasdaq-100: CTSH) is one of the world's leading professional services companies, transforming clients' business, operating and technology models for the digital era. Our unique industry-based, consultative approach helps clients envision, build and run more innovative and efficient businesses. Headquartered in the U.S., Cognizant is ranked 185 on the Fortune 500 and is consistently listed among the most admired companies in the world. Learn how Cognizant helps clients lead with digital at www.cognizant.com or follow us @Cognizant.
💡 Quick Summary
Seeking a career-building opportunity? The Cognizant is hiring for certified Veeva developers position is now open for candidates interested in the Software Developer Jobs sector. This role in Chennai offers a professional environment and growth potential.
Requirement Snapshot: Candidates should possess basic communication skills, a proactive attitude, and the ability to work in a team. Experience in Software Developer Jobs is a plus.
