Packaging Process Engineer

2 weeks ago


Tampa, Florida, United States Lonza Full time

Lonza is a prominent player in the life sciences sector, operating globally across multiple continents. Our success is driven by our talented workforce, who collaborate to create innovative solutions that benefit businesses and improve lives. We empower our employees to take charge of their careers, fostering an environment where ideas—both large and small—can lead to meaningful change.

We are currently seeking a Packaging Process Engineer to oversee the design and execution of all GMP manufacturing processes, ensuring compliance and efficiency. This role involves managing the technical and regulatory components of various projects from start to finish. The Packaging Process Engineer will work collaboratively across departments to ensure that all initiatives align with Lonza's strategic objectives.

Key Responsibilities:

  • Offer technical expertise for all GMP packaging processes, equipment, and related projects.
  • Conduct process validation for commercial packaging, including the development and execution of validation protocols.
  • Identify, specify, and procure GMP packaging equipment, including setup and qualification processes.
  • Engage in project scheduling activities in coordination with relevant departments.
  • Draft, review, and approve Standard Operating Procedures (SOPs), specifications, and necessary documentation.
  • Contribute to budget forecasting and assist in managing departmental expenditures.
  • Collaborate with maintenance teams for equipment installation, repairs, and preventive maintenance tasks.
  • Perform various duties to support change requests, deviations, investigations, CAPA initiatives, and operational enhancements.
Qualifications:
  • Bachelor's degree in Engineering is strongly preferred; extensive experience may be considered in lieu of formal education.
  • Proficient in problem identification, data collection, and solution development.
  • Adept at interpreting technical instructions and managing multiple variables.
  • Capable of handling multiple projects and meeting deadlines effectively.
  • Strong ability to read and understand technical documents, including operations manuals and SOPs.
  • Excellent technical writing skills for producing reports, qualification protocols, and other documentation.
  • Solid mathematical and computer skills are essential.
  • A minimum of 3 years of relevant experience is required.
  • Experience in Pharma cGMP, Life Sciences, Consumer Products, Biotechnology, or Chemical industries is necessary.

At Lonza, we recognize the impact our products and services have on millions of lives, and we take this responsibility seriously. Our commitment to ethical practices is paramount, as we believe that success is only meaningful when achieved with integrity.

Our employees are drawn to Lonza for the intellectual challenges and the opportunity to innovate within the life sciences field. In return, we provide the fulfillment that comes from making a significant difference in the world.



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