Director Supply Chain Product Life Cycle Management

Let's do this. Let's change the world. We are seeking an enterprise-minded Supply Chain leader who can lead an integrated, high-performing Lifecycle Management (LCM) organization across Europe, Latin America and Canada (ELMAC), and translate global strategy into disciplined regional execution.

In this vital role, you will lead the Regional LCM organization for ELMAC within the Global LCM HUB. You will be accountable for regional launch and post-approval lifecycle strategy, portfolio execution, performance and capability across Europe, Middle East and Africa (EMEA), Latin America and Canada (LACAN). You will lead Regional Operations teams and partner closely with Manufacturing Sites, Product Lifecycle Teams (PLTs), Global Product Development Teams (PDTs), Regulatory Affairs, Quality, Planning, Commercial and Affiliate organizations to ensure launches and lifecycle changes are delivered on time, compliantly and with uninterrupted supply to patients.

You will establish a common operating model across ELMAC, create clear decision ownership and handoffs with the Global LCM HUB, and represent regional needs in Global LCM Governance. The role provides leadership for a regional organization of approximately 14 people. The role reports into the Global LCM HUB lead and you will be part of the Global LCM HUB management team.

In addition the role will have a dotted reporting line to the Executive Director ELMAC Supply Chain and you will also be a member of their management team, playing a crucial role in the interaction with the ELMAC commercial organization regarding product launch and LCM events.

• Bachelor's degree in Supply Chain Management, Engineering, Life Sciences, Business or a related discipline.
• 12+ years of progressive experience in pharmaceutical or biotechnology Supply Chain, commercialization, product lifecycle management, manufacturing operations, regulatory operations or project/program leadership.
• Demonstrated senior leadership experience leading geographically dispersed teams and complex cross-functional portfolios in a global matrix environment.
• Strong knowledge of pharmaceutical product launches and post-approval lifecycle management, including CMC variations, labelling changes, SKU management and regional implementation.
• Experience operating in GMP-regulated environments, with a sound understanding of quality, regulatory and supply continuity requirements.
• Proven ability to establish governance, manage portfolio trade-offs and translate strategy into measurable execution performance.
• Exceptional stakeholder management, influencing, communication, analytical and problem-solving skills; fluent English, written and verbal.
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• Master's degree in Supply Chain Management, Engineering, Business or a related field.
• Experience working across EMEA, Latin America and/or Canada, including affiliate and distributor operating models.
• Experience with Product Lifecycle Teams, Global Product Development Teams, portfolio governance, S&OP/IBP and regional launch governance.
• Experience with SAP, lifecycle/portfolio management systems, Smartsheet, Power BI or comparable digital planning and performance tools.
• Lean, Six Sigma, Operational Excellence, PMP, PRINCE2 or equivalent certification.

• Enterprise leadership mindset with the ability to align diverse stakeholders behind a common outcome.
• Comfortable operating strategically, tactically and operationally in a changing and ambiguous environment.
• Decisive, collaborative and accountable; able to manage conflict constructively and drive timely resolution.
• Strong people-development capability and a track record of building inclusive, high-performing teams.
• Resilient and pragmatic, with a continuous-improvement mindset and uncompromising focus on patients, quality and delivery.

At 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. Amgen is advancing a broad and deep pipeline and portfolio of medicines to treat heart disease, obesity and obesity-related conditions, rare diseases, inflammatory conditions and cancer.  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.

DIRECTOR SUPPLY CHAIN PRODUCT LIFECYCLE MANAGEMENT ELMAC

• Set and deliver the ELMAC Lifecycle Management strategy, aligned with global product strategy, regulatory filing plans, commercial priorities and Global Supply Chain objectives.
• Lead the EMEA and LACAN Regional Product Management organizations, establishing clear objectives, accountabilities, capacity plans and performance expectations.
• Create a single, scalable regional way of working for launches, variations, SKU introductions and rationalizations, product discontinuations and other post-approval lifecycle activities.
• Define regional priorities and make timely trade-off decisions across the portfolio, escalating material risks and decisions through Global LCM Governance.
• Build a culture of ownership, collaboration, continuous improvement and patient focus across the ELMAC LCM organization.

• Ensure regional launch and lifecycle plans are developed and executed for new products, new presentations, strengths, devices, market expansions and post-approval changes.
• Ensure regional requirements, country readiness, supply implications and affiliate needs are incorporated into product and lifecycle plans at the appropriate decision points.
• Represent ELMAC Operations in Global PDTs, PLTs, Regional Operations Teams (ROTs), launch teams and relevant portfolio or commercialization governance forums.
• Partner with site LCM execution and other functional teams to ensure regional and technical readiness activities are integrated and deliver against agreed milestones.
• Ensure effective regional launch prioritization, including support for country business cases and filing or launch governance where required.

• Own end-to-end regional visibility of the ELMAC LCM portfolio, including timelines, dependencies, resource demand, risks, critical path and delivery outcomes.
• Ensure the appropriate high-touch or low-touch operating model is applied to each product, working with the LCM Capability teams to allocate work and preserve end-to-end product ownership.
• Ensure a single Regional Operations team and a single site LCM execution team own each lifecycle activity, minimizing handoffs and avoiding fragmented accountability.
• Drive timely resolution of regional barriers affecting CMC variations, labelling updates, artwork, master data, regulatory implementation, supply planning or market readiness.
• Maintain business continuity and patient supply by anticipating risks, leading mitigation plans and escalating issues that could impact supply, launch timing or compliance.

• Represent ELMAC in Global LCM Governance, ensuring regional priorities, risks, decisions and performance insights are visible and acted upon.
• Establish and review regional KPIs covering speed-to-market, lifecycle execution, handover quality, adoption, productivity, risk and compliance.
• Use performance data to identify systemic constraints, drive root-cause analysis and lead improvement initiatives across the ELMAC network.
• Deploy Global LCM HUB tools, standard processes, templates and handoffs across ELMAC, ensuring sustained adoption after transformation handback.
• Contribute to the LCM Community of Practice by sharing best practices, developing capability and strengthening consistency across regions, sites and partner organizations.

• Recruit, coach and develop ROL’s and product-support talent; build succession, capability and engagement plans for the organization.
• Balance resources and portfolio demand across EMEA and LACAN, ensuring capacity is focused on the highest business and patient-impact priorities.
• Build trusted senior partnerships with Global LCM, site leadership, Regulatory Affairs, Quality, Commercial, Planning, Affiliate Supply Chain and external partners.
• Communicate a clear regional portfolio narrative, including decisions, progress, risks and required actions, to senior stakeholders and governance forums.
• Lead through change in a complex global matrix, ensuring local requirements are understood while maintaining global standards and enterprise priorities.
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We are all different, yet we all use our unique contributions to serve patients. The experienced professional we seek is a leader with these qualifications.

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’ll support your journey every step of the way.

In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards.

As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of 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. We make all employment decisions without regard to race, color, religion, sex or any other characteristic protected by applicable law.

We provide reasonable accommodations to applicants and employees with disabilities, consistent with legal requirements. Please contact us to request accommodation.