Regulatory Affairs Intelligence Assoc Dir
2 weeks ago
Join Amgen’s Mission of Serving Patients
At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.
Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare Disease
- we reach millions of patients each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.
Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.
**Director, Global Regulatory Intelligence Team**
The Director leads the strategic development and execution of the Global Regulatory Intelligence (GRI) function, ensuring Amgen stays ahead of an evolving global regulatory landscape. This role defines the team's mission, sets priorities, leads cross-functional collaborations, and ensures high-impact intelligence is embedded into regulatory strategy across the enterprise.
**Key Responsibilities**:
- ** Function Leadership & Vision**:
Establish and evolve the Regulatory Intelligence function, defining structure, staffing strategy, vendor/outsourcing model, and the technology roadmap to support global operations. Set the vision and oversee the execution of intelligence deliverables that enable accelerated, compliant global product filings and approvals.
- ** Strategic Regulatory Insight & Change Leadership**:
Lead development of strategic insights into global regulatory trends and changes. Translate intelligence into actionable internal guidance, influencing filing strategies, development plans, and Amgen’s engagement with evolving regulatory expectations. Serve as senior advisor on emerging regulatory shifts, coordinating enterprise-level change response strategies.
- ** External Engagement**:
Build and maintain relationships with external regulatory intelligence networks, peer companies, industry associations, and regulatory agencies to enhance Amgen’s proactive intelligence-gathering capabilities. Coordinate with Regulatory Policy and country affiliates to ensure early awareness of critical developments.
- ** Cross-Functional Integration**:
Partner with Global Regulatory Affairs, Regulatory CMC, Clinical, Safety, and Policy functions to integrate intelligence into product strategy, labeling, and lifecycle plans. Lead cross-functional initiatives where regulatory intelligence enables enterprise transformation (e.g., structured submissions, digital requirements).
- ** Team Management & Talent Development**:
Hire, develop, and lead a high-performing Regulatory Intelligence team (including direct reports and external partners). Set goals, manage performance, mentor staff, and build capabilities aligned with future-state regulatory operations. Define and oversee budget, resource allocation, and vendor management for the function.
- ** Operational Excellence & Innovation**:
Ensure efficient, scalable, and continuously improving intelligence operations. Drive the adoption of innovative tools, data analytics, and automation solutions to accelerate and enhance regulatory intelligence outputs.
**Knowledge & Skills**:
- ** Regulatory Expertise**:
Deep knowledge of global regulatory systems and evolving frameworks across major and emerging markets. Experience identifying and interpreting high-impact regulatory changes and their implications for development, submission, and approval strategies.
- ** Strategic & Analytical Thinking**:
Demonstrated ability to connect regulatory developments with strategic business impacts. Able to assess ambiguity, provide direction under uncertainty, and influence cross-functional decisions.
- ** External Presence & Influence**:
Skilled in representing Amgen in industry forums and engaging with regulatory bodies. Able to distill complex global issues into clear, compelling messaging for senior stakeholders.
- ** Leadership & Communication**:
Proven leadership of cross-functional teams and direct staff. Strong ability to communicate complex regulatory concepts clearly and persuasively across senior, technical, and global audiences.
- ** Innovation & Operational Mindset**:
Experience with process optimization, digital tools, and knowledge management systems. Ability to modernize intelligence workflows using structured data and automation.
**Qualifications**:
- ** Education**:
Doctorate degree and 4+ years of experience, or Master’s degree and 15+ years, or Bachelor’s degree and 16+ years in regulatory affairs, policy, intelligence, or a related field.
- ** Experience**:
- Prior leadership experience in globa
-
Assoc. Dir. Ddit Dev Regulatory Affairs
3 days ago
Hyderabad, Telangana, India Novartis Full time**Summary**: The role of Service Delivery Associate Director in Hyderabad focuses on leading the strategic and operational implementation of Veeva Vault in Regulatory Affairs, ensuring alignment with organizational goals and regulatory compliance. This position requires extensive experience in project leadership, data migration, Validation and testing, and...
-
Assoc. Dir. DDIT DEV Regulatory Affairs
3 weeks ago
Hyderabad, India Novartis Full timeJob Description SummaryThe role of Service Delivery Associate Director in Hyderabad focuses on leading the strategic and operational implementation of Veeva Vault in Regulatory Affairs, ensuring alignment with organizational goals and regulatory compliance. This position requires extensive experience in project leadership, data migration, Validation and...
-
Regulatory Affairs Intelligence Assoc Dir
2 weeks ago
Hyderabad, Telangana, India Amgen Full time**India - Hyderabad** **JOB ID**: R-218756 **ADDITIONAL LOCATIONS**: - India - Hyderabad **WORK LOCATION TYPE**: On Site **DATE POSTED**: Jun. 30, 2025 **CATEGORY**: Regulatory Join Amgen’s Mission of Serving Patients At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living...
-
Assoc. Dir. DDIT DEV Regulatory Affairs
1 week ago
Hyderabad, Telangana, India Novartis Full time ₹ 12,00,000 - ₹ 36,00,000 per yearSummaryThe role of Service Delivery Associate Director in Hyderabad focuses on leading the strategic and operational implementation of Veeva Vault in Regulatory Affairs, ensuring alignment with organizational goals and regulatory compliance. This position requires extensive experience in project leadership, data migration, Validation and testing, and cutover...
-
Assoc. Dir. Ddit Dev Ra Sol. Del
4 weeks ago
Hyderabad, Telangana, India Novartis Full timeSummary As Assoc Dir DDIT DEV RA Sol Del you will create the detailed IT solution service design based on functional specifications to meet quality and performance requirements and technical constraints Responsible for detailed design development and delivery of system solutions for Regulatory Affairs RA You will engage with global business leaders and...
-
▷ [Immediate Start] Assoc. Dir. Ddit Dev Ra Td
4 weeks ago
Hyderabad, Telangana, India Novartis Full timeSummary As Assoc Dir DDIT DEV RA TD you will create the detailed IT solution service design based on functional specifications to meet quality and performance requirements and technical constraints Responsible for detailed design development and delivery of system solutions for Regulatory Affairs RA You will engage with global business leaders and leverage...
-
Assoc. Dir. DDIT DEV RA TD
3 weeks ago
Hyderabad, India Novartis Full timeJob Description SummaryAs Assoc. Dir. DDIT DEV RA TD you will create the detailed IT solution/service design, based on functional specifications to meet quality and performance requirements and technical constraints. Responsible for detailed design, development, and delivery of system solutions for Regulatory Affairs (RA). You will engage with global...
-
Assoc. Dir. DDIT DEV RA Sol. Del.
3 weeks ago
Hyderabad, India Novartis Full timeJob Description SummaryAs Assoc. Dir. DDIT DEV RA Sol. Del. you will create the detailed IT solution/service design, based on functional specifications to meet quality and performance requirements and technical constraints. Responsible for detailed design, development, and delivery of system solutions for Regulatory Affairs (RA). You will engage with global...
-
Assoc. Dir. DDIT DEV RA Sol. Del
3 weeks ago
Hyderabad, India Novartis Full timeJob Description Summary As Assoc. Dir. DDIT DEV RA Sol. Del. you will create the detailed IT solution/service design, based on functional specifications to meet quality and performance requirements and technical constraints. Responsible for detailed design, development, and delivery of system solutions for Regulatory Affairs (RA). You will engage with global...
-
Assoc. Dir. DDIT DEV RA Sol. Del
1 week ago
Hyderabad, Telangana, India Novartis Full time ₹ 12,00,000 - ₹ 36,00,000 per yearSummaryAs Assoc. Dir. DDIT DEV RA Sol. Del. you will create the detailed IT solution/service design, based on functional specifications to meet quality and performance requirements and technical constraints.Responsible for detailed design, development, and delivery of system solutions for Regulatory Affairs (RA). You will engage with global business leaders...