A

Amgen

Makes biotech medicines for serious illnesses

Manager, Web Partnerships and Enablement

Program ManagementPosted on Nov 13
Full-timeRemote in USARemote

About the Job

Requirements

  • A doctorate degree and 2 years of digital or web program, project, governance, and technology experience; or a master's degree and 4 years of such experience; or a bachelor's degree and 8 years of such experience; or an associate's degree and 10 years of such experience.
  • Experience establishing or applying web standards, governance, launch readiness, and operating models across multiple business functions, platforms, or markets.
  • Experience advising senior and cross-functional partners, translating business needs into web recommendations, and evaluating platform, vendor, or capability options.
  • Knowledge of Agile methodologies, preferably SAFe, and experience managing website roadmaps and continuous improvement initiatives.
  • Proficiency with program or project management tools such as Workfront, AEM, JIRA, ServiceNow, Confluence, and Google Analytics.
  • Experience managing end-to-end digital and website lifecycle projects in fast-paced, multi-stakeholder environments, including complex, cross-country, and high-impact initiatives.
  • Ability to negotiate priorities, manage expectations, and build productive relationships across diverse cross-functional teams and external partners.
  • Experience in regulated industries, preferably pharmaceutical, with understanding of compliance requirements; familiarity with accessibility standards such as WCAG, privacy regulations such as GDPR and US consumer laws, web technologies such as HTML and CSS, and industry best practices is a plus.
  • Experience developing detailed project documentation and translating business requirements into technical specifications.
  • Ability to communicate and collaborate across functions, explain complex technical concepts clearly to non-technical stakeholders, connect enterprise web capabilities and standards to business needs, balance business needs with compliance, resource, and platform constraints, surface risks early, and work across time zones when required.

Responsibilities

  • Guide web portfolio governance and provide launch readiness support for Medical, Corporate Affairs, Clinical Trials, R&D, and approved non-commercial web initiatives by clarifying governance requirements, decision points, owners, readiness needs, and appropriate web delivery processes.
  • Serve as a subject-matter expert on content management systems, design systems, back-end system integrations, pharmaceutical web marketing best practices, and emerging trends; advise business teams on applying web capabilities to business objectives and audience needs, identify opportunities to strengthen digital experiences, translate business goals into strategic recommendations, define future-state capability enhancements and roadmaps, and partner with business, technology, content, design, analytics, and agency teams to assess feasibility, value, and dependencies.
  • Promote adoption of enterprise web standards and governance; assess externally hosted or custom web platforms and help plan transitions toward global web enterprise standards, aligning scope, dependencies, risks, and stakeholder responsibilities.
  • Advise teams on engaging web vendors and agencies; support statement-of-work development and procurement planning for web services, including analytics and search engine optimization engagements, in coordination with procurement and business partners.
  • Lead quarterly intake and prioritization of web initiatives with Technology and business stakeholders, aligning investment with enterprise strategy, business value, and resource capacity; translate prioritized needs into scope, requirements, sequencing, timelines, and delivery plans; assess cross-project and platform dependencies, clarify ownership, and apply governance to support informed prioritization and delivery.
  • Lead cross-functional web initiatives from approved plans through development, launch, and hypercare; coordinate creative and content handoffs, development, approvals, quality assurance and user acceptance testing, deployment, and production validation; align timelines, resources, budgets, dependencies, and release requirements; establish launch readiness, facilitate decisions, resolve issues, and communicate status and escalations to support timely delivery.
  • Monitor program health, governance adherence, documentation, risks, issues, and change impacts across web initiatives; coordinate business, content, creative, development, technology, analytics, and agency partners to clarify ownership, manage handoffs, and resolve conflicts across concurrent initiatives, platform migrations, technology releases, and regulatory deadlines; embed legal, regulatory, privacy, accessibility, brand, and operational resilience requirements throughout delivery, escalating material risks as needed.
  • Partner with analytics and search engine optimization teams to interpret web traffic, user behavior, search performance, and other digital insights and use findings to recommend website optimization; lead structured retrospectives and apply performance insights, lessons learned, and emerging trends to recommend improvements to web capabilities, standards, tools, templates, and delivery processes; scale effective practices to improve consistency, efficiency, collaboration, and speed to market.

Desired Qualifications

  • Six or more years of experience managing end-to-end digital and website lifecycle projects in fast-paced, multi-stakeholder environments, including complex, cross-country, and high-impact initiatives.
  • Experience with Agile methodologies, preferably SAFe, and project management tools such as Workfront, AEM, JIRA, ServiceNow, Confluence, and Google Analytics.
  • Experience operating in regulated industries, preferably pharmaceutical, and familiarity with WCAG accessibility standards, GDPR, US consumer privacy laws, HTML/CSS, and industry best practices.

About the Company

Amgen

Makes biotech medicines for serious illnesses

Amgen develops and makes biologic medicines, which are drugs built from proteins and antibodies grown in living cells, for serious conditions such as heart disease, cancer, and bone loss. Its anemia drug Epogen, approved in 1989, became one of the biotechnology industry's first blockbuster medicines. Amgen grows these drugs in large tanks called bioreactors, and its products include the cholesterol drug Repatha, the bone-building drug Evenity, and the severe asthma drug Tezspire. It earns money by selling these medicines, mostly through large drug wholesalers that supply hospitals and pharmacies. Amgen was founded in 1980 and is based in Thousand Oaks, California.

Company size
10,001+
Company stage
IPO
Headquarters
Thousand Oaks, CA
Founded
1980

Recently Posted Jobs

Explore more opportunities at Amgen

See more jobs