Sr Associate – Digital Governance
Location: Hyderabad, India
Job ID: R-219154
Posted On: July 1, 2025
Employment Type: Full-Time | On-Site
About Amgen:
Amgen is a global biotechnology leader that uses advanced science and technology to fight the world’s toughest diseases. For over four decades, we’ve led the way in biopharma innovation—pushing the boundaries of medicine and delivering transformative therapies to millions of patients worldwide.
About the Role:
As a Sr Associate – Digital Governance, you will be a key contributor to the Global Regulatory Affairs and Strategy team, supporting digital compliance across Amgen’s web and social media platforms. You’ll help maintain accurate digital records, ensure database integrity, support regulatory readiness, and assist in driving digital compliance across the organization. This hybrid-regulatory-technical role requires strong attention to detail, collaboration skills, and adaptability to shifting business needs.
Key Responsibilities:
Maintain and ensure the accuracy of Amgen’s global digital site inventory database.
Support compliance tracking for global websites, social media assets, and digital projects.
Respond to process-related inquiries and guide stakeholders on digital governance best practices.
Assign mandatory training to digital asset managers and support users across functions.
Perform quality control audits on digital asset entries and database consistency.
Collaborate with Domain Law team to manage and register Amgen URLs.
Identify compliance risks, participate in inspections, and support corrective action plans.
Generate and maintain weekly and quarterly reports, including status updates and task completions.
Provide project and change management support for governance initiatives.
Update SOPs, training materials, and guidance documents as needed.
Test and validate contact information for digital sites to ensure ongoing compliance.
Required Skills & Experience:
Strong working knowledge of Veeva PromoMats and digital asset tracking systems.
Excellent verbal and written communication skills with meticulous attention to detail.
Familiarity with pharmaceutical regulatory requirements (US and global).
Hands-on experience with Excel, project coordination, and compliance documentation.
Understanding of social media management and digital project workflows.
Flexible to work in shift-based hours, including occasional overnight support for US launches.
Preferred Qualifications:
Prior experience in Regulatory Affairs or Pharmacovigilance functions.
Working knowledge of change management and project management practices.
Familiarity with digital campaign compliance and social media processes in regulated environments.
Master’s or Bachelor’s degree in life sciences, digital governance, or a related field.
Education Requirements:
Master’s degree
OR
Bachelor’s degree with 3+ years of related experience
OR
Associate’s degree with 5+ years of related experience
Estimated Salary: ₹10–14 LPA (based on role complexity, regulatory environment, and pharma sector benchmarks)
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