US Regulatory Lead

BioSpace; Washington (District of Columbia); On-site; USD 150,000 - 190,000; Full time

Job summary

Amgen is seeking a US Regulatory Lead to plan and execute regulatory strategies for its products across the United States. You will coordinate with cross‑functional teams to manage submissions, labeling, and lifecycle activities while interfacing with regulatory agencies.

The role requires extensive US regulatory experience, leadership skills, and a strong understanding of FDA processes to drive timely approvals and ongoing compliance.

Qualifications

• Doctorate degree required for regulatory leadership.
• Experience in US regulatory strategies and submissions preferred.
• Strong leadership and cross-functional collaboration skills required.
• Excellent communication and negotiation abilities.
• In-depth knowledge of US regulatory landscape and FDA processes.

Responsibilities

• Lead regulatory strategies for Amgen products in the US.
• Plan and manage regulatory submissions and lifecycle activities.
• Coordinate with global teams on regulatory plans and labeling.
• Interact with US regulatory authorities and respond to inquiries.
• Ensure local labeling and product compliance with all regulations.
• Mentor junior regulatory staff and drive process improvements.

Skills

US Regulatory experience

Leadership experience

Regulatory submissions

Communication skills

Drug development knowledge

FDA familiarity

Education

Doctorate degree

Masters degree + 3 years US Regulatory experience

Bachelors + 5 years US Regulatory experience

Associates + 10 years US Regulatory

High school diploma / GED + 12 years US Regulatory

Job description

Join Amgens Mission of Serving Patients

At Amgen, if you feel like youre part of something bigger, its because you are. Our shared missionto serve patients living with serious illnessesdrives all that we do.

Since 1980, weve helped pioneer the world of biotech in our fight against the worlds 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, youll 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, youll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.

US Regulatory Lead

What you will do

Lets do this. Lets change the world. US Regulatory Affairs provides country regulatory expertise and execution for the development, registration, and lifecycle management of all Amgen molecules.

The Local Regulatory Representative (Manager) is assigned to one or more Amgen products, and plans and executes the Regulatory strategies for that product(s) in their country(ies). The product(s) assigned have medium complexity programs/strategies and medium impact to Amgen.

Assist in aligning local regulatory requirements with Amgens corporate standards.

Provide local input to and execute regulatory strategies.

Plan and manage local regulatory submissions in compliance with corporate standards and local regulatory requirements.

Provide guidance on local mechanisms to optimize product development and regulatory approvals.

Ensure local labels are developed and maintained in line with local legislation and Amgen standards and procedures.

Ensure and support local regulatory product compliance (eg, IMR, PMCs, and agency commitments).

Act as the point of contact with regulatory agencies.

Support and provide input into the global regulatory strategy for assigned products, including Global Regulatory Strategic Plans, labeling documents, etc.

Strategic and Execution

Contributes for the filing plan (MA and Lifecycle maintenance), advising and discussing with the local cross-functional team.

With general supervision, executes the filing plan (MA and Lifecycle maintenance) for their country(ies), where applicable.

Ensures regulatory submissions are made on time and meet Amgens corporate and local regulatory requirements.

Creates, reviews, and approves source text for country labeling, and owns the country artwork based on source text.

Collaborates with Regional and Global Study Operations (GSO) teams to support local planning and execution for clinical studies in accordance with national legal and regulatory requirements (where appropriate).

Reviews and approves the promotional and non-promotional materials.

Monitors changes in the local Trade Associations/national legislation and forwards information to local/regional groups communicating the impact to Amgen.

Monitors the external regulatory environment to help inform/advise in the regulatory decision making.

Ensures/supports regulatory product compliance (e.g. IMR, PMCs, pediatric and other agency commitments).

Manages the regulatory submission of urgent safety communications, DHPCs & DILs as required by Amgen SOPs or local regulatory requirements, as needed.

Advises Global teams on local regulatory implications and requirements relevant to the global clinical development/Marketing Applications plans and objectives.

As part of the Global Regulatory Team (GRT), provides regulatory direction/expertise on local regulatory mechanisms to optimize product development (e.g., expediting studies, Orphan Drug Designations, expedited regulatory designations, compassionate use, and pediatric plans).

Health Authority Interactions

Acts as the point of contact with regulatory agencies in fulfilling local obligations.

Participates/contributes to local agency interactions and their preparation.

Communication and Collaboration

Works closely with cross-functional colleagues in the country, Affiliate or Hub to align on strategy and deliver country/Affiliate/Hub goals.

Exchanges regulatory information and intelligence with other regulatory colleagues and cross functional teams on an ongoing basis and provides advice on local regulatory considerations/regulations in a timely manner.

Partners with International Regulatory Leads (IRLs) and Global Regulatory Leads (GRLs) to support the regulatory development, registration, and lifecycle management of all Amgen molecules.

Partners with peers to ensure consistency on procedures.

Acts as contact and create relationships with Agency staff on specific product assignment (if applicable).

Establishes regular contacts and interactions with Distributors (if applicable).

Provide SME support to process improvement projects/initiatives.

Country Specific Activities

Assists locally in Healthcare Compliance activities where applicable.

Participates in local regulatory process improvements, initiatives and training.

Oversees external vendor/contractor relationships where applicable.

Assists locally in Healthcare Compliance, QA or pharmacovigilance activities where applicable.

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.

Mentoring

Mentors and/or advises other(s) Local Regulatory Representatives at more junior levels.

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The dynamic professional we seek is a leader with these qualifications.

Basic Qualifications

• Doctorate degree
• Masters degree and 3 years of US Regulatory experience
• Bachelors degree and 5 years of US Regulatory experience
• Associates degree and 10 years of US Regulatory experience
• High school diploma / GED and 12 years US Regulatory

In addition to meeting at least one of the above requirements, you must have experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation or resources. Your managerial experience may run concurrently with the required technical experience referenced above.

Preferred Qualifications

• Understanding of drug development.
• Knowledge of Regulatory principles.
• Regulatory submissions experience and experience interacting with regulatory agencies (FDA)
• Working knowledge of U.S. legislation/regulations relating to medicinal products and applicable regulatory principles.
• Comprehensive understanding of regulatory activities and how they impact other projects and/or processes.
• Knowledge and experience in the US regulatory environment relevant for product area and development stage.
• Demonstrate strong teamwork 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.
• Working with policies, procedures, and SOPs.
• Cultural awareness and sensitivity to achieve results across both regional, country and international borders.

What you can expect from us

As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well‑being. From our competitive benefits to our collaborative culture, we will support your journey every step of the way.

The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.

In Addition To The Base Salary, Amgen Offers a Total Rewards Plan, Based On Eligibility, Comprising Of Health And Welfare Plans For Staff And Eligible Dependents, Financial Plans With Opportunities To Save Towards Retirement Or Other Goals, Work/life Balance, And Career Development Opportunities That May Include

• A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
• A discretionary annual bonus program, or for field sales representatives, a sales‑based incentive plan
• Stock‑based long‑term incentives
• Award‑winning time‑off plans
• Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.

In any materials you submit, you may redact or remove age‑identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.

Application Deadline

Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.

Sponsorship

Sponsorship for this role is not guaranteed.

As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.

Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.