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Config Specialist- Veeva Vault (Regulatory Submission/RIMS)

Hoffmann-La Roche

based on 1 Review

3-7 years

Pune

1 vacancy

Config Specialist- Veeva Vault (Regulatory Submission/RIMS)

Roche Holding

posted 5mon ago

Key skills for the job

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As an Enterprise DevOps Engineer, you will join the Enterprise Engineering cluster in the Product Development, Integration and Engineering chapter, you will partner with other internal experts, specializing in various aspects of Enterprise engineering
Together, the team collaborates on multiple products that contribute to Roches internal business requirements
As a DevOps Engineer, you will be accountable for developing, optimizing, and managing IT services/applications in Veeva with focus on Regulatory submission management
You will also focus on ensuring cost-effectiveness, scalability, and security in all aspects of the digital product lifecycle, including maintenance activities
As part of enterprise engineering, you will be involved in understanding the business application processes and functions

Your key responsibilities :

Lead, collaborate, and facilitate cross-functional experts to deliver a particular solution with a good understanding of the business requirements.
Responsible for the quality of the technical deliverables, which also includes peer reviews.
Develop and publish the application/prototype with the knowledge of DevOps according to the underlying infrastructure.
Lead the implementation and maintenance of efficient Continuous Integration / Continuous Delivery pipelines to automate the delivery process.

Act as a subject matter expert for Veeva to support the design, implementation and maintenance of reliable and performant integrations.

Your qualifications and experience:

Understanding of Veevas architecture, data models and integration methods.
Proficiency in configuration tools and methodologies specific to Veeva
Knowledge of integration mechanisms, data flow and efficient communication between applications.
Certification of the Veeva platform will be value-added.
Regulatory Submission Process: Understanding of regulatory submission processes, regulatory requirements, and standards like Good Clinical Practice.
Essential effective oral and written communication skills in English.
Working knowledge of Computer Systems Validation (CSV) and GxP.
Working knowledge of regulations like HIPAA and GDPR in the healthcare industry.
Beneficial is to have knowledge of cybersecurity best practices in the context of clinical data.
Moderate travel is required and the ability to work across multiple time zones.

Education / Years of Experience:

3-5 Years of relevant work experience with bachelors degree in Computer Science/IT/Engineering or 5 - 7 Years of relevant work experience
At least 3+ years experience of working in one or more multinational work environments (eg life science industry experience is a plus).
Good analytical thinking and problem-solving skills
Good communication and collaboration skills
Good understanding of regulatory compliance and security