Programme Manager Lead

AbbVie Inc.; Leinster; Hybrid; EUR 110,000 - 140,000; Full time

Job summary

AbbVie Inc. is seeking a Programme Manager Lead to provide governance, coordination, and execution oversight across CDQ projects.

You will establish PMO practices, prioritize initiatives, and ensure timely delivery while guiding cross-functional teams and communicating with senior leadership. The role requires 10+ years of industry experience with at least 5 years in program management within a regulated pharmaceutical setting, strong GMP knowledge, and excellent stakeholder engagement.

Qualifications

• Bachelor’s degree in Science, Engineering, Business, or a related field.
• 10+ years of industry experience, including 5+ years in program or project management.
• Experience managing large, cross-functional pharmaceutical projects.

Responsibilities

• Lead the CDQ PMO function coordinating project managers and resources to drive function and enterprise-wide project success and ensure cross-functional alignment.
• Establish and maintain project governance, prioritization, and reporting processes across assigned cross-functional teams and CDQ Functional Teams.
• Translate PMO and business priorities into clear execution plans, milestones, dependencies, and tracking mechanisms.
• Monitor project progress, risks, issues, actions, and dependencies; escalating blockers and resource needs as appropriate.
• Develop and maintain standard templates, tools, dashboards, and metrics to support consistent program management practices.
• Lead and coordinate cross-functional teams to support the execution of complex programs, including planning, implementation, and budget tracking where applicable.
• Ensure timely, clear, and consistent communication to stakeholders, including senior leadership, on program status, risks, decisions, and next steps.
• Support the development and rollout of standard program management processes, training, and ways of working across the organization.
• Facilitate governance forums, communities of practice, and communication channels that enable alignment and knowledge sharing.
• Oversee assigned team members, including workload coordination and support for delivery of their responsibilities.
• Maintain alignment with relevant project standards, business requirements, and organizational governance expectations.
• Support continuous improvement of project management processes, tools, and operating rhythms.

Skills

Project governance

Cross-functional collaboration

Stakeholder communication

Strategic planning

Risk management

Education

Bachelor's degree (Science/Engineering/Business)

Job description

Company Description

About AbbVie

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn,Facebook,Instagram,XandYouTube.

Job Description

The Programme Manager Lead is responsible for providing governance, coordination, and execution oversight across assigned projects within CDQ (Commercial Distribution Quality). The role establishes and maintains consistent project management practices, supports prioritization and decision-making, and ensures delivery against agreed milestones, scope, and timelines. The position also leads cross-functional collaboration, facilitates stakeholder communication, and oversees assigned projects to support effective execution and alignment with business objectives.

• Leads the CDQ PMO function coordinating project managers and resources to drive function and enterprise-wide project success and ensure cross-functional alignment
• Establish and maintain project governance, prioritization, and reporting processes across assigned cross-functional teams and CDQ Functional Teams.
• Translate PMO and business priorities into clear execution plans, milestones, dependencies, and tracking mechanisms.
• Monitor project progress, risks, issues, actions, and dependencies; escalating blockers, decisions, and resource needs as appropriate.
• Develop and maintain standard templates, tools, dashboards, and metrics to support consistent program management practices.
• Lead and coordinate cross-functional teams to support the execution of complex programs, including planning, implementation, and budget tracking where applicable.
• Ensure timely, clear, and consistent communication to stakeholders, including senior leadership, on program status, risks, decisions, and next steps.
• Support the development and rollout of standard program management processes, training, and ways of working across the organization.
• Facilitate governance forums, communities of practice, and communication channels that enable alignment and knowledge sharing.
• Oversee assigned team members, including workload coordination and support for delivery of their responsibilities.
• Maintain alignment with relevant project standards, business requirements, and organizational governance expectations.
• Support continuous improvement of project management processes, tools, and operating rhythms.

Qualifications

• Bachelor’s degree in Science, Engineering, Business, or a related field.
• 10+ years of relevant industry experience, including 5+ years in program or project management.
• Demonstrated experience managing large, complex, cross-functional projects in a pharmaceutical or similarly regulated environment.
• Strong knowledge of GMP manufacturing, supply chain, CMC technical development, and pharmaceutical regulations.
• Proven ability to develop governance models, manage priorities, and drive execution across multiple stakeholders.
• Strong communication, organization, analytical, presentation, and interpersonal skills.
• Demonstrated ability to resolve conflicts and influence cross-functional teams and technical experts.
• Ability to understand technical aspects of complex systems and contribute to detailed problem-solving discussions.

Additional Information

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html