Amgen Supply Chain Manager – Variation Lead in Thousand Oaks, California
HOW MIGHT YOU DEFY IMAGINATION?
You’ve earned your degree. How will you use that achievement to reach your goals? Do more with the knowledge you’ve worked hard to acquire and the passion you already have. 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, reaching over 10 million patients worldwide. Become the professional you are meant to be in this meaningful role.
Supply Chain Manager - Variation Lead
What you will do
Let’s do this. Let’s change the world. In this vital role you will be accountable for driving the cross-functional strategy of a portfolio of variation projects for Amgen’s commercial products. The position will be a phenomenal opportunity to further help craft and establish the young organization building a hard-working team and capability. Holistically, this group focuses on robust project, portfolio, and process management for variations to capture and accelerate the value of change to our commercial products.
Effective management of variations (post-launch changes to Amgen’s commercial products) is critical. This is especially true given the forecasted growth in Amgen’s product portfolio and international expansion. Drivers of variations vary and include, but are not limited to: scale up, tech transfer, supplier driven changes required to ensure supply, manufacturing network strategy, new or improved product presentations, test method revisions, regulatory commitments, responses to patient safety issues, and operational excellence projects.
The Variation Lead is accountable for driving cross-functional execution of a portfolio of variation projects. The Variation Lead partners with impacted stakeholders to further establish the young organization, build high-performing teams, and continually improve the end-to-end variation management process. Holistically, this group focuses on robust project, portfolio, and process management to capture and accelerate the value of change to our commercial products.
The scope of the variation management process includes: proposal submission, business case development supporting business case governance approval, prioritization within the holistic variation portfolio, project planning, and project execution.
Represent the Variation Management Organization (VMO) as a core team member of multiple Product Delivery Teams (PDTs) to guide teams through the process, integrating inputs across Process Development, Regulatory, Supply Chain, Manufacturing, Quality, etc. into cohesive execution and implementation strategies
Optimize the product’s overall Life Cycle Management strategy to minimizing variation complexity and implementation cycle times
Lead business case development; a few examples of VMO-led business cases include drug substance/drug product process improvements, drug product expiry extensions, and method revisions
Lead cross-functional stakeholders in development of variation project plans (defining required technical activities, change control strategy, supply strategy, and regulatory strategy through submission and approval from global regulatory agencies)
Drive end-to-end execution of a PDT’s portfolio of variation projects (from business case through global regulatory approvals) by ensuring key Technical, Regulatory, and Supply Chain milestones complete per plan
Partner with stakeholders including Manufacturing sites, Quality Control and External Supply for PDT visibility into upcoming changes; enabling proactive management and implementation of variations
Communicate priorities to product, functional, and regional stakeholders. Identify risks and risk mitigation plans, resolve issues, and escalate to appropriate governance as needed.
Adhere to processes and best practices set by Business Process Owner, drive continuous improvement of processes. Standardize and integrate project management tools; establish single source of truth for variation status.
Shepard variations through the governance process
Lead the Variation Execution Team (VET) meeting within Supply Chain to ensure dynamic Regional inputs and constraints are reflected in the Global Supply transitions plan
Periodic travel to sites required up to 10%.
What we expect of you
We are all different, yet we all use our unique contributions to serve patients. The operations/supply chain professional we seek is a self-starter with these qualifications.
Master’s degree and 2 years of Operations or Regulatory experience
Bachelor’s degree and 4 years of Operations or Regulatory experience
Associates degree and 8 years of Operations or Regulatory experience
High school diploma / GED and 10 years of Operations or Regulatory experience
6 plus years biotech or pharmaceutical operations experience
Able to facilitate and influence senior clients and partners
Able to successfully manage workload to timelines
Familiarity with basic project management tools
Ability to negotiate a strategic position after taking feedback from multiple sources
Strong project management, problem-solving, and analytical skills; experience with project management tools
Demonstrated ability to lead cross-functional teams, consistently deliver on-time, and ensure high-quality results
Collaborates and communicates well with others, able to balance divergent inputs from various stakeholders and drive issue resolution
Ability to operate in a matrixed or team environment with site, functional, and executive leadership
Experience driving decision making using DAI principles
Some experience with a “variation management” process
Periodic travel to sites required up to 10%.
Some of the vast rewards of working here
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.
Full support and career-development resources to expand your skills, enhance your expertise, and maximize your potential along your career journey
A 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—with compensation and benefits rated above 4 stars (out of 5) on Glassdoor
for a career that defies imagination
Objects in your future are closer than they appear. Join us.
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.
If you're seeking a career where you can truly make a difference in the lives of others, a career where you can work at the absolute forefront of biotechnology with the top minds in the field, you'll find it at Amgen.
Amgen, a biotechnology pioneer, discovers, develops and delivers innovative human therapeutics. Our medicines have helped millions of patients in the fight against cancer, kidney disease, rheumatoid arthritis and other serious illnesses.
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 but compete intensely to win. Together, we live the Amgen values as we continue advancing science to serve patients.
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, or disability status.