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Job Description

HOW MIGHT YOU DEFY IMAGINATION?

If you feel like you’re part of something bigger, it’s because you are. At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together—researching, manufacturing, and delivering ever-better products that reach over 10 million patients worldwide. It’s time for a career you can be proud of. Join us.

Regulatory Affairs Director

Live

What you will do

Let’s do this. Let’s change the world. Amgen is seeking a Regulatory Affairs Director supporting products in the General Medicine Therapeutic Area. Global Regulatory Affairs (GRA) provides global regulatory leadership, expertise, and execution for the development, registration, and life cycle management of all Amgen molecules.

In this vital, product-facing role you will lead the Global Regulatory Team (GRT) in the Regulatory Affairs organization. The purpose of Regulatory Affairs Director is:

• To lead GRTs within Amgen’s GRAAS organization
• To develop a comprehensive regulatory strategy that takes into account worldwide regulatory requirements to drive product development, global registration, achievement and maintenance of desired regional labeling, and effective regulatory agency interactions
• To provide regulatory expertise and guidance to product teams

The responsibilities of the Regulatory Affairs Director position are:

• Develop and implement the global regulatory product strategy
• Lead GRTs
• Represent Regulatory on the product team and other key commercialization governance bodies
• Develop Global Regulatory Strategic Plan and provide regulatory input into the product’s Global Strategic Plan.
• Acquire feedback from the GRT members to develop a global regulatory strategy that supports product development, registration, and lifecycle maintenance. Identify and communicate regulatory risks
• Represent GRA on the product team
• Develop registration strategies and plans aimed at achieving regulatory approval and product labeling
• Provide regulatory direction in the development of the core datasheets to align commercial objectives in the context of available and expected scientific data, regulatory guidance, and precedent
• Facilitate planning and implementation of global regulatory filings (e.g. clinical trial applications, marketing applications, label extensions, CMC changes)
• Ensure consistency of evidence-based global product communication (e.g. regulatory submission documents)
• Monitor and assess the impact of relevant global regulations, mentorship, and current regulatory environment
• Ensure guidance on regulatory mechanisms to optimize product development (e.g. expediting FIH studies, Orphan Drug, Fast Track, conditional /accelerated approval, compassionate use, and pediatric plan) is assessed and incorporated into the global regulatory strategy
• Communicate consistently well defined, successful regulatory strategies throughout the organization such that expectation is understood
• Ensure effective regulatory agency communications by leading core regulatory and cross-functional teams (e.g. GRTs, filing teams)
• Attend key regulatory agency meetings which could impact the global product strategy
• Represent Amgen Regulatory on external partnership teams at the product level

While this position is based in Thousand Oaks, a remote work arrangement will be considered.

Win

What we expect of you

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

Basic Qualifications:

• Doctorate degree and 4 years of regulatory experience in biotech or science, OR
• Master’s degree and 8 years of regulatory experience in biotech or science, OR
• Bachelor’s degree and 10 years of regulatory experience in biotech or science

Preferred Skills:

• Ability to lead and build effective teams
• Strong communication skills - both oral and written
• Ability to understand and communicate scientific/clinical information
• Can anticipate and mitigate against future strategic issues & uncertainties
• Capability to resolve conflicts and develop a course of action
• Has cultural awareness and sensitivity to achieve global results
• Planning and organizing abilities
• Successfully prioritizes to handle multiple activities/projects simultaneously
• Capability to make complex decisions and address challenges effectively
• Ability to deal with ambiguity
• Organizational savvy
• Negotiation skills

Thrive

What you can expect of us

As we work to develop treatments that take care of others, so we work to care for our teammates’ professional and personal growth and well-being.

• Vast opportunities to learn and move up and across our global organization
• Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
• Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

Apply now for a career that defies imagination

In our quest to serve patients above all else, Amgen is the first to imagine, and the last to doubt. Join us. careers.amgen.com

Equal Opportunity Statement

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.

We will ensure that individuals with disabilities are provided a 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 an accommodation.