Join Amgen’s Mission of Serving PatientsAt 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.Compliance Manager, Program Effectiveness & AssessmentWhat you will doLet’s do this. Let’s change the world. In this vital role, you will support the global compliance program with measuring effectiveness, gathering data, and analyzing information to implement a strategy to measure the effectiveness of our Ethics & Compliance program.The Manager will report to the Director of Global Program Effectiveness and Insights in Worldwide Compliance and Business Ethics (WC&BE). You will lead and support on the process and program management of designing, building and maintaining Amgen’s Compliance-related metrics and key performance indicators. This will involve developing standardized processes and repeatable workflows to establish the success of effectiveness across WC&BE programs, working with internal and external stakeholders to compliance, and identifying, collecting and analyzing key data to develop and complete a strategy for assessing and evaluating each element of Amgen’s Ethics and Compliance program.Responsibilities include:
Support the development and execution of Compliance Program Effectiveness, ensuring alignment with regulatory requirements and industry standard processes.
Assist in the planning and execution of Amgen’s annual global risk assessment program, supporting the identification, evaluation, and mitigation of key compliance risks.
Identify key compliance areas, define and map key requirements, and analyze data to enhance program effectiveness, providing insights to strengthen compliance. Focus areas include policies and procedures, training, communications, business ethics, reporting, investigations and monitoring, processes, technology, and overall program execution.
Support a data-driven effective compliance program by working with stakeholders in compliance and other functions to gather data and information that underpin critical metrics and reporting under program effectiveness for the WC&BE leadership team and other relevant leadership teams.
Assist in monitoring external industry trends and developments in the regulatory environment, working across WC&BE, to support how to update and adapt the programmatic build to measure effectiveness and drive continuous improvement including best practices and industry guidance.
Stay informed on regulatory developments, industry trends, and emerging best practices to refine and evolve the compliance program.
Collaborate with internal teams to optimize compliance processes, enhance capabilities, and integrate technology and automation to improve program efficiency.
Work across teams and cross-functional areas to establish and track compliance metrics, generate reports and insights for leadership to measure program performance and effectiveness.
Domestic travel up to 20% for business-related activities may be required.Location: While hybrid from accessible commute to Amgen Thousand Oaks, CA is preferred, this role may also be in a remote capacity with some expected travel.What we expect of youWe are all different, yet we all use our unique contributions to serve patients. The compliance professional we seek is an innovative leader with these qualifications.Basic Qualifications:Doctorate degreeORMaster’s degree and 2 years of Compliance, Legal, Audit, Monitoring, Regulatory or similar experienceORBachelor’s degree and 4 years of Compliance, Legal, Audit, Monitoring, Regulatory or similar experienceORAssociate’s degree and 8 years of Compliance, Legal, Audit, Monitoring, Regulatory or similar experienceORHigh school diploma / GED and 10 years of Compliance, Legal, Audit, Monitoring, Regulatory or similar experiencePreferred Qualifications:
5-8 years of experience in pharmaceutical/biotech industry experience, particularly in Compliance, Legal, Audit, Monitoring, Regulatory Affairs.
Possess strong working knowledge of compliance program frameworks, risk assessment methodologies, and regulatory requirements.
Strong interpersonal and customer engagement skills, with the ability to work cross-functionally and present findings clearly.
Ability to analyze complex compliance data, identify trends, and generate meaningful insights for leadership.
Strong collaborator and problem solver.
High ability to research and compile trends and information from disparate sources.
Experience working with management and partners to manage processes, and provide strong business management fundamentals in day-to-day work.
Agile and able to adjust to ambiguity, complexity and changing directions quickly to meet urgent business needs.
Working knowledge and understanding of Office of Inspector General (OIG) Compliance Program Guidance for Pharmaceutical Manufacturers, Pharmaceutical Research and Manufacturers of America (PhRMA) Code, U.S. Federal Anti-Kickback Statute (AKS), False Claims Act (FCA), current Corporate Integrity Agreements (CIAs), Accreditation Council for Continuing Medical Education (ACCME) guidelines, Prescription Drug Marketing Act (PDMA), FDA commercial guidelines, U.S. Federal and State data privacy laws and regulations, U.S. Federal and State transparency reporting requirements, similar laws and regulations in countries outside the U.S., and other relevant laws and regulations.
Understanding of sales, marketing, value & access, product promotion, disease education, device regulatory, clinical research, and healthcare compliance.
Ability to initiate, handle, prioritize, and follow through on a high volume of work.
Past managerial experience directly managing people and/or leadership experience leading teams, projects, programs or directing the allocation of resources.
High familiarity and experience with Microsoft Word, Excel, PowerPoint and working with document repositories.
What you can expect of usAs 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’ll 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, including remote and hybrid work arrangements, where possible
Apply nowfor a career that defies imaginationObjects in your future are closer than they appear. Join us.careers.amgen.comIn 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 deadlineAmgen 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.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.