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Lonza

Global life sciences contract manufacturer

MSAT Associate Principal Engineer

Bioprocess & BiomanufacturingPosted on Nov 10
Full-timePortsmouth, NH, USANo salary listedIn-person

About the Job

Requirements

  • A Bachelor's, Master's, or PhD degree in Chemical Engineering, Biochemical Engineering, Biotechnology, Biology, Chemistry, or a related scientific discipline.
  • Significant experience in Manufacturing Science and Technology (MSAT), process transfer, technology transfer, process support, or biopharmaceutical manufacturing.
  • Strong expertise in deviation investigations, root cause analysis, data interpretation, and structured problem-solving methodologies.
  • Demonstrated ability to lead technical projects and influence cross-functional teams in a GMP-regulated environment.
  • Experience evaluating process changes, change controls, and manufacturing impacts on process performance and product quality.
  • Working knowledge of current Good Manufacturing Practice (cGMP) regulations, quality systems, regulatory expectations, and commercial biologics manufacturing operations.

Responsibilities

  • Lead process transfer and process support activities for commercial manufacturing processes while driving continuous improvement of MSAT practices and procedures.
  • Provide technical leadership to cross-functional teams to address complex manufacturing, process performance, and product quality challenges.
  • Evaluate process changes, major deviations, and post-release issues for impact on manufacturing performance and product quality.
  • Conduct advanced root cause investigations using structured problem-solving tools and lead implementation of effective corrective and preventive actions.
  • Assess new technologies and manufacturing approaches for suitability and process fit within the production environment.
  • Interface directly with customers through IPT, JPT, JTT, and Joint Steering Committee meetings, providing technical updates and support while escalating significant business or operational risks when appropriate.
  • Author and review technical documentation, support change control assessments, participate in customer and regulatory audits, and represent MSAT across site and customer-facing initiatives.

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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