Amgen Principal Engineer - Operations Core Content Lead in Thousand Oaks, California
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 read over 10 million patients worldwide. It’s time for a career you can be proud of. Join us.
Principal Engineer - Operations Core Content Lead (CCL)
What you will do
Let’s do this. Let’s change the world. . In this vital role you will be part of Amgen’s Final Product Technologies (FPT) Organization where you will be accountable to define strategic boundaries (core content) for platform technologies and advance overall platform execution strategy as part of Amgen’s efforts to expand our platform-based approach to product development. The CCL will represent FPT and Operations in gathering input of key partners across the organization, determining core content, and in determining key business processes for its implementation. The CCL will provide expert mentorship to product teams on platform strategies. The CCL will give voice and drive awareness to the generation and application of the core content.
Lead establishment of platform strategic boundaries for final product presentations, including drug delivery device, package and label, and container technologies
Drive awareness and adoption of the boundary framework across all platforms
Manage ongoing improvement of the core content to match the evolving needs of portfolio
Provide mentorship to product programs moving through platform governance
Lead / drive assessment of change impact and fit-to-platform against boundaries
Budget responsibility and other program assignments as applicable
What we expect of you
We are all different, yet we all use our unique contributions to serve patients. The engineer we seek is successful and multi-functional collaborator with these qualifications.
Doctorate degree and 2 years of Life Sciences Engineering experience
Master’s degree and 6 years of Life Sciences Engineering experience
Bachelor’s degree and 8 years of Life Sciences Engineering experience
Associate’s degree and 10 years of Life Sciences Engineering experience
High school diploma / GED and 12 years of Life Sciences Engineering experience
Master’s Degree or PhD in Mechanical, Electrical, Systems, Materials, Biomedical or similar technical field
10+ years of demonstrated experience in drug / device combination product or drug delivery development with broad exposure to HW/SW/ Systems design and technical depth in a technical field
5+ years of leadership experience in development, research, or manufacturing environment
Product design/development (design control) from concept to post product launch for Europe (EU MDR/CE Mark) & US submissions
Capable of concurrently working on different projects in a deadline driven environment
Demonstrated ability to partner with technical leadership team to implement product platform/subsystem multi-generation technology plan for a global program/product
Strong background in detailing requirements and specification for regulatory approval
Demonstrated strength in execution of product verification and validation, Design of Experiments (DOE)/SPC, process optimization & validation (IQ, OQ, PQ), Failure Mode Effects Analysis (FMEA)
INCOSE certification or formal Systems Engineering training/certification
Proficient experience driving Critical to Quality (CTQ) hierarchical decomposition (flow-down) to subsystems and components
Experience in platform-based system design and architecture
Strong oral and written communications
Experience in addressing and resolving system level architecture design trade-offs, tolerance/performance analysis, etc.
Robust knowledge of Quality Management System, Quality Management Policy and applicable laws and regulations
Practical experience in configuration management and change control process/requirements – CCB (change control board), CIT (change implementation team) concepts
Prior experience in management of contract resources
Experience in leading continuous improvement activities
Strong interpersonal skills
Familiar with the following standards: US Good Manufacturing Practices (21 CFR Part 4, 21 CFR 210/211, 21 CFR 820); Needle-based Injection Systems (ISO 11608-1); Quality Management (ISO 13485); Risk Management (ISO 14971); EU Medical Device requirements (EU MDR 2021); Medical Electrical Equipment (EN 60601)
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
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.
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.