Amgen – Manager – International Regulatory Lead Amgen

The Corporate Institute; Hyderabad; On-site; INR 2,500,000 - 4,200,000; Full time

Job summary

The Corporate Institute in Hyderabad, Telangana, seeks an International Regulatory Lead (Manager) to provide regulatory leadership for international countries for Amgen products, coordinating with global, regional and local teams.

The role focuses on developing international regulatory strategies, supporting registrations and lifecycle management, and driving cross-functional collaboration to ensure timely submissions and compliant labeling.

Qualifications

• Strong regulatory knowledge and principles.
• Experience with global/regional regulatory submissions.
• Ability to translate scientific data into regulatory strategy.
• Familiarity with CTAs, MAs and lifecycle management.

Responsibilities

• Advise Global teams on regulatory implications for development plans and objectives.
• Provide direction on international regulatory mechanisms to accelerate development.
• Plan regulatory submissions for products within the portfolio.
• Develop international regulatory strategy documents and communicate risks and contingencies.
• Lead label development and submission strategy with cross-functional teams.

Skills

Regulatory knowledge

Strategic thinking

Cross-functional leadership

Communication skills

Negotiation

Project management

Education

Doctorate degree

Master’s degree

Bachelor’s degree

Job description

About The Role

The International Regulatory Lead (IRL) Manager will provide regulatory leadership and expertise for International countries for one or more Amgen products. This role involves collaboration with various functions and local regulatory teams to optimize product development and regulatory approvals in International countries, develop international regulatory strategy, and provide regulatory support for in-country product registrations and life cycle management.

Job Summary

The International Regulatory Lead (Manager) is assigned to lead one or more Amgen products. The product(s) assigned have medium complexity programs/strategies and medium impact to Amgen.

• Provide Guidance and Leadership on mechanisms to optimize product development and regulatory approvals.
• Develop the international regulatory strategy and contribute to Global regulatory plans.
• Support regulatory product compliance (e.g. RIM, PMCs, ESC levels, and agency commitments).
• Support and advise on the local label strategy and alignment to cCDS/reference label.
• Build effective relationships and communication paths across global, regional, local and functional organizations.
• Enable efficiencies and seamless execution across the international countries.
• Contribute to process improvement projects, as assigned.

Key Activities

Strategy And Execution

• Advises Global teams on regulatory implications and requirements relevant to the global clinical development/Marketing Applications plans and objectives.
• Provides regulatory direction/expertise on the international regulatory mechanisms to optimize product development (e.g. expediting FIH studies, Orphan Drug Designation, expedited regulatory designations, compassionate use and pediatric plan).
• Under general supervision, plans regulatory submissions (e.g. clinical trial, marketing authorization applications and lifecycle management) for products within Amgen’s portfolio.
• Under general supervision, contributes to the development of international regulatory strategy documents (regulatory product filing plan, strategies, risks associated with the potential Agency outcomes and contingency planning, estimate likelihood of success) and communicates to others, as appropriate.
• Provides and maintains CTA/MA documentation. May author documents/redact documents to support a regulatory filing.
• Leads the internal discussions related with Agency meetings and in accordance with GRT strategy (and communicates outcomes back to GRT and others, as applicable).
• Directs the development of the international product label by collaborating with the Labeling Working Group to define commercial objectives in the context of available and expected scientific data, regulatory guidance, precedents and competitor labeling.
• Manages the international label submission strategy, leads the negotiation activities with cross-functional teams and is accountable for the label deviation requests and outcomes.
• Supports Local Regulatory teams in triaging queries from health authorities, and where appropriate, help identify existing responses to same or similar questions, leveraging knowledge management.
• Advises and supports other groups on the review of promotional and non-promotional materials, as needed.
• Supports process improvement initiatives and metrics.

Communication And Collaboration

• Participates as a member of the Global Regulatory Team (GRT), Evidence Generation Team (EGT), Labeling Working Group (LWG), Clinical Study Team (CST), and others, as applicable.
• Shares regulatory information and implications with the GRT and other Global teams on an ongoing basis and provides advice on international considerations. Participates in LWG/ELB meetings with advice on local deviation requests.
• Partners with the peers to agree on product strategy including projected submission and approval time.
• Maintains regular communications with the local teams to ensure alignment on strategy and keep the countries informed of status on the product development.
• Partners with peers to ensure consistency in procedures.
• Builds effective relationships and communication paths across the Global and Local elements of the GRAAS function.

Regulatory Research

• Maintains an awareness of new and developing legislation, regulatory policy and technical Regulatory guidance relating to Amgen products.
• Performs regulatory research to obtain relevant histories, precedence and other information relevant to regional product advancement.

Knowledge And Skills – Scientific And Technical

• Knowledge of Regulatory principles.
• Working with policies, procedures and SOP’s.
• Comprehensive understanding of regulatory activities and how they impact other projects and/or processes.
• General knowledge of national legislation and regulations relating to medicinal products.
• General awareness of the registration procedures/challenges in the region for CTAs, MAs and all lifecycle management activities.
• Knowledge and experience in the international regulatory environment relevant for product area and development stage.
• Understanding of drug development.

Others

• Demonstrate strong team work ability.
• Good communication skills – both oral and written.
• Good negotiation and Influencing skills.
• Ability to understand and communicate scientific/clinical information.
• Ability to resolve conflicts and develop a course of action leading to a beneficial outcome.
• Cultural awareness and sensitivity to achieve results across both regional, country and International borders.

Education And Experience (Basic)

• Doctorate degree and 6 years of directly related experience.
• OR.
• Master’s degree and 8 years of directly related experience.
• OR.
• Bachelor’s degree and 10 years of directly related experience.

Education And Experience (Preferred)

• 8 – 13 years of experience with degree and in-depth regulatory experience and/or related to the region.
• In-depth knowledge of regional countries legislation and regulations relating to medicinal products.

Location

Hyderabad, Telangana.

Category

Regulatory.

Job Type

Full time.