Custom Software Engineer
Bengaluru
Job No. atci-5211380-s1914286
Full-time
工作描述
Project Role : Custom Software Engineer
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 a highly experienced and strategic Veeva Vault Regulatory lead to manage, lead, and deliver Veeva Vault-based solutions for Regulatory operations. The ideal candidate will have 5+ years of IT experience with significant hands-on and leadership experience in the Life Sciences domain, specifically in implementing and supporting Veeva Vault Regulatory Suite (Submission , Publishing etc.).
The role involves cross-functional leadership, stakeholder engagement, vendor coordination, and end-to-end solution delivery in regulated environments. The candidate must bring a deep understanding of clinical trial processes, GxP compliance, and Veeva platform capabilities.
Roles & Responsibilities:
- Lead end-to-end implementation and management of Veeva Vault regulatory solution
- Serve as the primary point of contact for business stakeholders, ensuring alignment of IT solutions with clinical operational needs.
- Manage cross-functional project teams, including business analysts, developers and testers.
- Define and drive project plans, timelines, and deliverables, ensuring on-time and within-budget execution.
- Facilitate requirement gathering, gap analysis, and solution design for clinical operations use cases.
- Lead and support validation activities including creation and review of validation documentation (URS, IQ/OQ/PQ, test scripts).
- Maintain awareness of industry trends, Veeva releases, and regulatory changes impacting clinical systems.
Professional & Technical Skills:
- Must To Have Skills: Proficiency in Veeva Vault.
- Strong understanding of software development methodologies and best practices.
- Experience with system integration and data management.
- Ability to analyze and troubleshoot software issues effectively.
- Familiarity with project management tools and techniques.
Additional Information:
- The candidate should have minimum 5 years of experience in Veeva Vault.
- This position is based at our Bengaluru office.
- A 15 years full time education is required.
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 a highly experienced and strategic Veeva Vault Regulatory lead to manage, lead, and deliver Veeva Vault-based solutions for Regulatory operations. The ideal candidate will have 5+ years of IT experience with significant hands-on and leadership experience in the Life Sciences domain, specifically in implementing and supporting Veeva Vault Regulatory Suite (Submission , Publishing etc.).
The role involves cross-functional leadership, stakeholder engagement, vendor coordination, and end-to-end solution delivery in regulated environments. The candidate must bring a deep understanding of clinical trial processes, GxP compliance, and Veeva platform capabilities.
Roles & Responsibilities:
- Lead end-to-end implementation and management of Veeva Vault regulatory solution
- Serve as the primary point of contact for business stakeholders, ensuring alignment of IT solutions with clinical operational needs.
- Manage cross-functional project teams, including business analysts, developers and testers.
- Define and drive project plans, timelines, and deliverables, ensuring on-time and within-budget execution.
- Facilitate requirement gathering, gap analysis, and solution design for clinical operations use cases.
- Lead and support validation activities including creation and review of validation documentation (URS, IQ/OQ/PQ, test scripts).
- Maintain awareness of industry trends, Veeva releases, and regulatory changes impacting clinical systems.
Professional & Technical Skills:
- Must To Have Skills: Proficiency in Veeva Vault.
- Strong understanding of software development methodologies and best practices.
- Experience with system integration and data management.
- Ability to analyze and troubleshoot software issues effectively.
- Familiarity with project management tools and techniques.
Additional Information:
- The candidate should have minimum 5 years of experience in Veeva Vault.
- This position is based at our Bengaluru office.
- A 15 years full time education is required.
职位要求
15 years full time education
