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  1. All roles
  2. AstraZeneca PLC
  3. Associate Director, Product Lifecycle Management. Dublin, Athlone or Cork
AstraZeneca PLC logo
AstraZeneca PLC

Associate Director, Product Lifecycle Management. Dublin, Athlone or Cork

HybridBlanchardstown Road North, Dublin, IrelandApplications closedHealthTechB2B SaaS

Our Take

Drive product lifecycle strategy for RDU products at AstraZeneca, managing global supply chain and regulatory projects.

What you’ll do

  • Lead monthly LCM meetings with cross-functional teams
  • Manage Global S&OP LCM Portfolio Review
  • Act as gatekeeper for new product impacting projects
  • Collaborate with regulatory CMC on strategies
  • Track regulatory approvals for supply impacting changes
  • Drive change control strategy and project plans
  • Develop transition plans for LCM projects

What they’re looking for

  • 10+ years pharmaceutical industry experience
  • Experience in supply chain/technical development
  • Global and site-based LCM program management
  • Proficiency in Smartsheet and PM tools
  • Understanding of pharma supply chain processes
  • Experience with complex LCM programs (NPI, divestment)

What you get

  • Competitive salary and benefits package
  • Opportunities for professional development
  • Collaborative and innovative work environment
  • Focus on rare diseases and patient impact
  • Flexible working arrangements
  • Commitment to diversity and inclusion

Skills & Focus Areas

  • product lifecycle management
  • program management
  • project management
  • Smartsheet
  • supply chain
  • regulatory CMC
  • GMP
  • lean philosophy

As posted by AstraZeneca PLC

Are you ready to take on a pivotal role in the Alexion Product Management Team within Global Supply Chain & Strategy? As the Associate Director of Product Lifecycle Management, you'll be at the forefront of delivering the LCM strategy for RDU products. This position requires you to align, lead, and collaborate across functional barriers, establishing program governance to ensure the progress and timely implementation of Supply Impacting and/or New Market registration projects. You'll be responsible for driving the life cycle management governance, ensuring effective monthly product life cycle meetings, and collaborating with Strategic Product Leads to deliver the operations life cycle strategy.

Accountabilities:• Set up and lead monthly Product Life Cycle Management meetings with cross-functional teams to review active LCM events for RDU commercial products.• Lead the Global S&OP LCM Portfolio Review, communicating program status, deviations, and risks.• Act as the gatekeeper for new product impacting projects, partnering with various business functions for onboarding.• Collaborate with regulatory CMC to develop regulatory strategies and track project landmarks.• Track regulatory approvals of changes identified as Supply Impacting and/or New Market Registration.• Drive agreement on change control strategy and maintain project-related change controls.• Deliver and maintain detailed transition plans for LCM projects with Global Supply Chain.• Plan and track changeover/transition activities and project implementation milestones.• Define and establish master data strategy with Master Data Governance.• Identify potential risks and elaborate contingency plans with relevant collaborators.• Support Strategic Product Leads with project prioritization and endorsement.• Provide product-specific overviews/dashboards to the Product Management Team.• Align with Project Leads and authorities from different functions for effective collaboration.• Ensure compliance with GMP, regulatory requirements, EHS, and continuous improvement of quality processes.• Handle, communicate, and resolve critical issues related to product lifecycle management globally.• Drive product lifecycle management philosophy within AO and embed principles within associated teams.

Essential Skills/Experience:• Bachelor's degree in business or scientific field required. Advanced degree a plus.• 10+ years of experience handling and leading multiple complex projects/programs within the pharmaceutical industry across various functions e.g., supply chain / production and/or technical development.• Must be able to create a highly collaborative and inclusive environmconstantly evolvingent necessary for the cross-functional teams to be effective.• Intercultural experience and ability to act in a complex and constantly evolving business environment.• Excellent knowledge of program and project management discipline and its application to product lifecycle management at a global and site-based level.• Great knowledge of Smartsheet and other Project Management tools/systems.• Consistent track record in completing effective program management skills in cross-functional matrix organizations.• Strong understanding of pharmaceutical industry supply chain processes and lean philosophy.• Ability to bridge between scientific, technical, and business functions for effective collaboration and driving results.• Demonstrated success in creating and handling product life cycle programs of high complexity (NPI, pruning, divestment, integration).• Ability to effectively implement the tools and techniques of the program and project management field, such as the development and management of multi-disciplinary program level integrated plans, critical path management, project risk management, decision analysis and meeting management.• Excellent level presentation skills and polished written and oral communication ability.• Ability to engage with senior management in Operations and cross-functionally.• Consistent record of achievement and delivery of team goals.• Strong understanding of Regulatory landscape desirable.• Knowledge of clinical and commercial manufacturing and distribution issues that impact project/product strategy and planning desirable.

Desirable Skills/Experience:• Bachelor's degree in business or scientific discipline required. Advanced degree a plus.• 10+ yrs. equivalent multi / cross functional experience.

When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.

At AstraZeneca, you'll find an environment where innovation thrives! Our commitment to rare diseases means embracing opportunities that are anything but ordinary. With a rapidly expanding portfolio, you'll enjoy an entrepreneurial spirit that fosters autonomy while connecting deeply with patients' journeys. Our culture celebrates diversity, innovation, and connection to patient experiences. Here, your career is not just a path but a journey to making a difference where it truly counts.

Ready to make an impact? Apply now to join our team!

Date Posted

15-Jun-2026

Closing Date

28-Jun-2026

Our mission is to build an inclusive and equitable environment. We want people to feel they belong at AstraZeneca and Alexion, starting with our recruitment process. We welcome and consider applications from all qualified candidates, regardless of characteristics. We offer reasonable adjustments/accommodations to help all candidates to perform at their best. If you have a need for any adjustments/accommodations, please complete the section in the application form.

Heads up: this role is no longer open for new applications.

We keep the page live for context and search continuity, but the apply action has been disabled.

Location
Blanchardstown Road North, Dublin, Ireland
Work mode
Hybrid
Track
Manager
Type
FULL_TIME
PostedJun 19
AstraZeneca PLC logo
AstraZeneca PLC
astrazeneca.com

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