Job Description

Project Role :

Software Development Lead

Project Role Description :

Develop and configure software systems either end-to-end or for a specific stage of product lifecycle. Apply knowledge of technologies, applications, methodologies, processes and tools to support a client, project or entity.

Must have skills :

Veeva Vault

Good to have skills :

NA

Minimum

5

year(s) of experience is required

Educational Qualification :

15 years full time education



Summary: We are seeking an experienced and motivated Team Lead with strong expertise in Veeva Vault RIM (Regulatory Information Management) and data migration projects within the life sciences or pharmaceutical domain. The ideal candidate will lead end-to-end implementation and migration efforts, ensuring timely delivery, quality, and alignment with regulatory requirements. Roles & Responsibilities: - Lead the implementation and configuration of Veeva Vault RIM modules (Registrations, Submissions, Submissions Archive, Product, and Health Authority). - Manage data migration lifecycle: planning, data mapping, extraction, transformation, loading (ETL), and validation from legacy systems to Veeva Vault RIM. - Collaborate with cross-functional teams including regulatory, QA, IT, and business stakeholders. - Define and manage project plans, timelines, resources, and deliverables. - Ensure compliance with regulatory standards (e.g., FDA, EMA) and Veeva best practices. - Act as the point of contact for issue resolution, escalations, and stakeholder communication. - Guide a team of analysts and developers; provide coaching, task assignment, and performance feedback. - Participate in solution design sessions, configuration workshops, UAT, and post-go-live support. - Support the creation of functional and technical documentation including - SOPs, configuration specs, and migration strategy documents. Monitor and report progress, risks, and mitigation strategies to leadership. Professional & Technical Skills: - 7-9 years of total experience with minimum 3-5 years of hands-on experience in Veeva Vault RIM implementation and/or migration. - Proven experience in leading data migration projects involving Veeva Vault or similar regulatory systems. - Strong understanding of Regulatory Affairs processes and global health authority requirements. - Experience with Veeva Vault Admin/config tools and Veeva migration tools (e.g., Vault Loader, Vault APIs). - Excellent communication and stakeholder management skills. - Familiarity with GxP compliance, 21 CFR Part 11, and validation requirements. - Experience in Agile or hybrid project methodologies. - Strong analytical and problem-solving abilities. -Veeva Vault RIM Certification(s). -Experience in life sciences consulting or working with top-tier pharma clients. -Exposure to integration projects involving Veeva Vault (e.g., with RIM, - PromoMats, Quality). - Knowledge of tools like ETL platforms, SQL, Excel macros, or custom migration scripts. Additional Information: - Work on cutting-edge Veeva Vault implementations for global clients. - Opportunity to lead impactful projects in the regulatory transformation space. - Collaborative and growth-oriented environment.




15 years full time education