#R-201076
opment portfolio. In this position, you will work with CRO/CMO's to support development, clinical/commercial manufacture, and business management. You will also lead the implementation of sourcing initiatives and manage a variety of external projects engaging domestic, international, and emerging market suppliers.
The responsibilities of this role include:
Project leadership of synthetic peptide and oligonucleotide external projects spanning development and clinical/commercial manufacture in close coordination with internal technical stakeholders
Ability to work under minimal guidance to manage of multiple assignments and/or business processes
Ability to build and maintain positive relationships with internal technical stakeholders to increase overall efficiency and success of programs
Supplier evaluation and outsourcing management including site selection activities
Development of scopes of work in close partnership with technical leads
Assurance that projects and/or programs meet results, compliance, speed, quality, and cost
Management of purchase orders, financial forecasting, and associated budget for externalization to adhere to financial targets and systems
Ability to establish and maintain external collaborations to monitor supplier performance, continuously improve efficiency, and ensure effectiveness of suppliers
Ability to independently identify project optimization opportunities (e.g., timeline, budget, technical completion)
Ability to clearly present analyses and articulate recommendations to Senior Management
Occasional domestic and international travel to support project results
What we expect of you
We are all different, yet we all use our unique contributions to serve patients. The experienced professional we seek is a strategic problem solver with these qualifications.
Basic Qualifications:
Doctorate degree and 2 years of engineering, science or business management experience OR
Master's degree and 4 years of engineering, science or business management experience OR
Bachelor's degree and 6 years of engineering, science or business management experience OR
Associate's degree and 10 years of engineering, science or business management experience OR
High school diploma/GED and 12 years of engineering, science or business management experience
Preferred Qualifications:
Advanced degree in engineering or science
Demonstrated understanding of drug development and commercialization for synthetic therapeutics, particularly synthetic peptides and oligonucleotides. This includes route scouting, raw material and starting material procurement, API/drug substance manufacture, process development, process engineering, and process characterization
Experience working with domestic and international CMOs/CROs
Solid understanding of cGMP, Regulatory/CMC, legal, quality requirements, and import/export policies
Self-starter with a high-level of comfort with ambiguity and complexity and the ability to multi-task while consistently delivering quality results
Experienced leader and team member of cross-functional and matrixed teams
Effective written, presentation, organizational, interpersonal, and influencing skills to address a broad scope of audiences including demonstrated ability to drive decision-making
Demonstrated quantitative and qualitative skills to support business process development, financial analysis, continuous improvement, operational excellence, performance management, and product lifecycle management
Proven business acumen with high-level strategic thinking
Strong problem-solving skills with the ability to structure, pragmatically scope, and solve complex problems
Thrive
Some of the vast rewards of working here
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.
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
Apply now
for a career that defies imagination
Objects in your future are closer than they appear. Join us.
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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 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.
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