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Lonza

Global life sciences contract manufacturer

Manufacturing Manager

Bioprocess & BiomanufacturingPosted on Nov 6
Full-timePortsmouth, NH, USA

About the Job

Requirements

  • Experience leading manufacturing operations within biopharmaceutical, biologics, cell therapy, or related GMP-regulated environments.
  • Demonstrated leadership experience managing teams, organizational change, hiring, training, and employee development.
  • Experience supporting technical transfers, project execution, and commercialization of manufacturing processes.
  • Strong knowledge of current Good Manufacturing Practice (cGMP) requirements, quality systems, deviation management, and manufacturing compliance expectations.
  • Experience with biological manufacturing operations, including fermentation, purification, drug product filling, freezing operations, or related modalities.
  • Strong business acumen, customer focus, collaboration, and ability to drive results in a fast-paced manufacturing environment.
  • Excellent communication, stakeholder management, and cross-functional collaboration skills.
  • Proven ability to manage priorities, budgets, continuous improvement initiatives, and operational performance metrics.

Responsibilities

  • Provide a safe, controlled work environment and ensure site safety objectives are communicated and understood by all manufacturing personnel.
  • Lead manufacturing teams and serve as the subject matter expert for assigned operations, including Cell Growth, Drug Product Filling, and related manufacturing processes.
  • Provide in-suite oversight during critical manufacturing activities such as harvest, vial filling, visual inspection, and other key production operations.
  • Support technical transfer activities, including process execution, methods transfer, engineering runs, training runs, water runs, and qualification activities.
  • Collaborate with Quality Assurance and cross-functional teams to establish procedures, quality systems, and manufacturing strategies for new and existing programs.
  • Partner with Internal Project Teams (IPTs), Joint Project Teams (JPTs), customers, and stakeholders to transfer and maintain processes in the manufacturing facility.
  • Own and manage manufacturing-related deviations, change controls, and lessons learned activities while supporting continuous improvement initiatives.
  • Support hiring, development, training, and performance management of manufacturing staff while fostering a high-performing team culture.
  • Collaborate with Manufacturing Technical Managers to identify equipment, material, and resource requirements needed to support production operations.
  • Partner with leadership to ensure accurate financial reporting, project progression, proposal support, and operational execution across Cell Therapy programs.
  • May serve as delegate for the Manufacturing Director during periods of absence.

Desired Qualifications

  • Experience with automated drug product filling systems utilizing restricted access barrier systems (RABS) and/or isolator technology.
  • Experience with automated or manual visual inspection systems.

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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