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Amgen Technology Private Limited

Manager Information Systems - docuBridge

8-13 Years
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  • Posted 7 days ago
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Job Description

Roles & Responsibilities:

  • Collaborate with internal Regulatory Operations stakeholders and vendor partner (Lorenz) to ensure accurate interpretation of requirements, compliant submission delivery, and successful deployment of the solution
  • Partner cross-functionally with Regulatory Affairs, Quality Assurance, IT Security, and vendor teams to gather detailed business requirements and convert them into scalable, compliant solutions
  • Define and manage project plans, resource allocation, timelines, and key deliverables across the entire lifecycle: assessment, procurement, configuration, validation, release, and support
  • Lead validation efforts by overseeing creation of validation plans, IQ/OQ/PQ protocols, and other documentation in alignment with GxP, 21 CFR Part 11, and Annex 11
  • Ensure submission readiness through structured document workflows, lifecycle management, and integration with systems like Regulatory Veeva Vault
  • Oversee user access, role-based privileges, and audit trail configurations to uphold system security and compliance
  • Own change control for the submission system aligned with ITIL, ensuring traceability for all changes, patches, and configurations
  • Develop training materials and deliver user training sessions for onboarding and system adoption
  • Monitor production performance, troubleshoot incidents with Lorenz, and resolve issues with minimal business impact
  • Drive continuous improvement initiatives to optimize usability, performance, and compliance
  • Track KPIs and provide leadership with regular updates on system performance, adoption, and throughput
  • Contribute to roadmap planning, identifying integration opportunities with tools like Lorenz eValidator and regulatory intelligence platforms
  • Serve as the SME for structured submissions during audits, inspections, and regulatory reviews
  • Rapidly prototype solutions and translate concepts into functional code
  • Adapt to agile methodology and lead cross-functional teams effectively
  • Utilize Jira and ServiceNow for project tracking and service management
  • Maintain technical documentation including design, deployment, operations, and disaster recovery
  • Monitor system health, performance, and capacity using dashboards and tracking tools
  • Implement and manage system security to guard against unauthorized access and vulnerabilities
  • Respond to and resolve incidents, conduct root cause analysis, and implement preventive solutions

Basic Qualifications:

  • Doctorate degree OR
  • Master's degree OR
  • Bachelor's degree with 8 to 13 years of relevant experience in Computer Science, IT, or related field

Must-Have Skills:

  • Deep understanding of pharmaceutical regulatory compliance (FDA, EU CTR, GxP)
  • Expertise with submission publishing systems, especially Lorenz docuBridge and Regulatory Veeva Vault
  • Strong experience managing technology initiatives and cross-functional teams
  • Proven ability to lead in dynamic, fast-paced environments with minimal supervision
  • Familiarity with methodologies like ITIL and Scaled Agile (SAFe)
  • Broad understanding of network technologies and IS architecture
  • Excellent stakeholder collaboration and communication skills

Good-to-Have Skills:

  • Knowledge of eCTD specifications and regulated system compliance
  • Prior leadership experience in pharma or tech organizations
  • Hands-on experience across the software development lifecycle of GxP systems
  • Working knowledge of SAFe, Agile frameworks, and change control management
  • Familiarity with IS governance practices and stakeholder alignment
  • Broader understanding of enterprise architecture and infrastructure domains

Professional Certifications:

  • ITIL (preferred)
  • SAFe for Teams (preferred)
  • Veeva Vault platform certification (preferred)

Soft Skills:

  • Strong analytical and troubleshooting capabilities
  • Effective verbal and written communication
  • Ability to manage multiple priorities with strong self-motivation
  • Team player with a collaborative mindset
  • Confident in presenting to diverse audiences and leadership

Shift Information:

  • Must be willing to work during evening or night shifts as required by business needs. This position may include second or third shift scheduling.

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Indian

About Company

Amgen harnesses the best of biology and technology to fight the world’s toughest diseases, and make people’s lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond what’s known today. Amgen is one of the 30 companies that comprise the Dow Jones Industrial Average, and we are also part of the Nasdaq-100 Index, which includes the largest and most innovative non-financial companies listed on the Nasdaq Stock Market based on market capitalization.

Job ID: 123277457