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Lonza

Global life sciences contract manufacturer

Manager, Program Management

Program ManagementPosted on Nov 13
Full-timePortsmouth, NH, USANo salary listed

About the Job

Requirements

  • A bachelor's degree in life sciences or a related discipline.
  • Significant program or project-management experience within a CDMO life sciences, biopharmaceutical manufacturing, or another complex matrix organization.
  • Demonstrated success leading cross-functional teams without direct authority.
  • Strong operational execution skills with attention to detail and follow-through.
  • Ability to manage competing priorities, frequent change, and complex stakeholder expectations.
  • Sound business judgment and experience managing project scope, schedules, risks, and customer commitments.
  • Customer relationship, communication, and conflict-resolution skills.
  • Ability to work independently, hold stakeholders accountable, and drive projects to completion.

Responsibilities

  • Lead tactical, operationally focused projects across two cell therapy assets.
  • Serve as the key interface between customers and cross-functional teams, representing customer priorities and ensuring effective execution.
  • Coordinate customer-driven changes and ensure actions, owners, and timelines remain on track.
  • Lead multidisciplinary project teams through influence, accountability, and clear communication.
  • Manage program scope, schedules, risks, issues, quality, and financial performance.
  • Establish governance, milestones, and escalation processes.
  • Identify potential obstacles and drive timely, practical solutions in a fast-moving operational environment.
  • Build relationships with customers, Account Management, site leadership, and functional partners.
  • Apply program-management tools and methodologies while sharing best practices across the organization.
  • Support asset stabilization and the program’s longer-term transition into a traditional customer-facing program-management model.

Desired Qualifications

  • Experience within a CDMO, biotechnology, or pharmaceutical environment.
  • A master’s degree, PMP, or another relevant project-management certification.

About the Company

Lonza

Global life sciences contract manufacturer

Lonza is a global provider of development and manufacturing services for the pharmaceutical, biotechnology, and nutrition sectors. It supports clients from early development through to commercial production, offering integrated processes such as process development, GMP manufacturing, formulation, fill-finish, and quality assurance to bring medicines and nutrition products to market. Lonza’s model is built on end-to-end CDMO capabilities, enabling companies to move from concept to scalable, compliant production with reliable supply chains. What sets Lonza apart is its long history and global footprint, combining decades of experience across chemistry, biology, and nutrition with a broad, end-to-end service network that supports projects from discovery to commercialization. The company aims to be a trusted, long-term partner in life sciences by helping customers efficiently develop and manufacture their products at scale while maintaining strict regulatory and quality standards.

Company size
10,001+
Company stage
IPO
Headquarters
Basel, Switzerland
Founded
1897

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