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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.
Regulatory Affairs Director - Inflammation and Rare Disease
What you will do
Let’s do this. Let’s change the world. Amgen is seeking a Regulatory Affairs Director supporting products in the Inflammation and Rare Disease 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 role of the Regulatory Affairs Director is to lead GRTs within Amgen’s GRAAS organization, 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, and to provide regulatory expertise and guidance to product teams.
The responsibilities of the Regulatory Affairs Director position are:
Develop and execute 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. Obtain input from the GRT members to develop a global regulatory strategy which 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 data sheet to align commercial objectives in the context of available and expected scientific data, regulatory guidance and precedent
Lead the 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 impact of relevant global regulations, guidance, 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
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 person 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 Qualifications:
Ability to lead and build effective teams
Strong communication skills - both oral and written
Ability to understand and communicate scientific/clinical information
Ability to anticipate and mitigate against future strategic issues & uncertainties
Ability to resolve conflicts and develop a course of action
Cultural awareness and sensitivity to achieve global results
Planning and organizing abilities
Able to prioritize and manage multiple activities
Ability to make complex decisions and solve problems
Ability to deal with ambiguity
Negotiation skills
What you can expect of us
As we work to develop treatments that take care of others, we also 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.
Full Time
Scientific Services
$194k-258k (estimate)
02/20/2024
05/15/2024
amgen.com
BOTHELL, WA
15,000 - 50,000
1980
Public
$10B - $50B
Scientific Services
Amgen discovers, develops, manufactures and delivers human therapeutics for patients suffering from serious illnesses.