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Process Development Product Lead

AmgenPottery Road, Dun Laoghaire, Co. Dublin, A96 F2A8Today
Dublin

Description

Career Category

Process Development

Job Description

Product Lead (Repatha), Process Development

Amgen Dun Laoghaire – Dublin

Overview:

The Product Lead (Repatha), Process Development is accountable for end-to-end product health stewardship and lifecycle delivery for Repatha at ADL. Reporting to the Sr. Manager, Process Development within the Product Portfolio Delivery (Syringe) team (Portfolio Management & Delivery), this role leads a cross-functional product team in a matrix organization to deliver technology transfers/new introductions and lifecycle management initiatives, while ensuring robust product governance, risk management, and alignment between site priorities and network demands.

Key responsibilities

Product health stewardship and governance

  • Act as the Product Health Steward for Repatha at ADL, owning product health through effective product governance and disciplined cross-functional leadership.
  • Lead and facilitate key Repatha project governance forums (e.g., team meetings, weekly/monthly product reviews) to ensure clear decisions, follow-up, and execution.
  • Ensure relevant site goals, network Governance Approved Baselines (GABs) and key governance decisions are translated into site action plans and prioritized appropriately.

Lifecycle strategy and delivery

  • Develop and maintain the site lifecycle management (LCM) program for Repatha, including scope definition, prioritization, and execution oversight across the product team.
  • Contribute to the long-term site product vision and strategy for Repatha, ensuring alignment with ADL strategy and network expectations.
  • Support new product/market introductions and Repatha SKU changes, coordinating readiness and execution across site functions.

Network interface & stakeholder leadership

  • Serve as ADL’s primary point of contact for Repatha Global Operations Leads (GOLs) and Product Delivery Teams (PDTs).
  • Ensure ADL needs, constraints, and priorities are clearly articulated and appropriately represented in site and global governance.
  • Build and maintain strong working relationships with product/process knowledge SMEs at both site and network level.

Risk management and technical transfer leadership

  • Own the site product risk register for Repatha; proactively identify vulnerabilities/gaps and drive mitigation and remediation plans through the product team.
  • Provide process transfer technical leadership and decision-making on Tech Transfer/NPI project team and within Technology Development & Transfer governance forums.
  • Influence site and above-site stakeholders to protect site strategy while meeting network commitments.

Compliance and quality expectations

  • Ensure all work is executed in alignment with cGMP, EHS, quality system requirements, and applicable business/financial controls.
  • Promote a culture of personal accountability, right-first-time execution, and proactive issue escalation.

Skills and knowledge

  • Strong matrix leadership capability: able to align cross-functional teams, drive decisions, and sustain execution without direct authority.
  • Solid understanding of development, manufacturing, validation, quality, regulatory, and product lifecycle management processes in a cGMP environment.
  • Demonstrated programme/project leadership skills (planning, risk management, governance, stakeholder alignment, and delivery tracking).
  • Clear, confident communication skills across site and global stakeholders; able to translate complexity into actionable decisions.
  • Strong interpersonal skills with demonstrated ability to influence, negotiate priorities, and manage competing demands.
  • Customer-focused, data-informed decision-making and strong prioritization skills across a dynamic portfolio.

Qualifications

  • Bachelor’s degree in a technical discipline required; Master’s degree or equivalent experience preferred.

Experience

  • 5–7 years’ experience in biopharma/pharma (cGMP environment), with demonstrated leadership in manufacturing/technical operations and cross-functional delivery.
  • Working technical knowledge relevant to Repatha manufacturing and lifecycle execution (e.g., parenteral fill-finish and/or primary packaging/combination product interfaces, as applicable).
  • Track record identifying risks/gaps and implementing practical mitigation/remediation plans through cross-functional teams.
  • Demonstrated technical and/or program leadership experience, including translating objectives into integrated, measurable execution plans.
  • Strong process and manufacturing execution background.

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