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Lonza

Global life sciences contract manufacturer

Packaging Engineer

Bioprocess & BiomanufacturingConfirmed live in the last 24 hours
Full-timeTampa, FL, USANo salary listed

About the Job

Requirements

  • Bachelor’s degree in Science, Engineering, or a related technical field.
  • Minimum 5 years of experience in a pharmaceutical cGMP environment.
  • Expertise in primary packaging design, material selection, packaging components, and packaging systems.
  • Experience with packaging technologies including vials, bottles, flexible bags, aseptic form/fill/seal systems, sterilization processes, labels, and single-use technologies.
  • Knowledge of process validation, stability studies, product interaction assessments, and shipping studies related to primary packaging.
  • Experience supporting GMP manufacturing operations, technology transfers, deviations, investigations, CAPAs, change controls, and continuous improvement initiatives.
  • Strong technical documentation skills, including preparation and review of Master Batch Records and qualification protocols, with the ability to collaborate effectively across cross-functional teams.

Responsibilities

  • Lead the design, selection, and optimization of primary packaging materials, components, and systems for GMP drug products.
  • Partner with Manufacturing, Quality Assurance, Supply Chain Operations, MSAT, and other stakeholders to deliver compliant and efficient packaging solutions.
  • Provide technical expertise for packaging technologies including vials, bottles, flexible bags, aseptic form/fill/seal systems, sterilization processes, labels, and single-use technologies.
  • Plan and support process validation, stability studies, product interaction assessments, and shipping studies related to primary packaging.
  • Drive continuous improvement and innovation initiatives focused on packaging performance, operational efficiency, lean principles, and GMP compliance.
  • Support technology transfers, change controls, deviations, investigations, CAPAs, and operational improvement programs.
  • Develop manufacturing documentation, review executed batch records, and support the qualification and implementation of GMP manufacturing equipment.

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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