MSAT Purification Lab Intern

LonzaVacaville, CA
2d$26 - $38Onsite

About The Position

We are actively recruiting candidates to participate in our 2026 On-site Internship program. This position is 12 weeks in length and will immerse you in the culture and operations of Lonza Vacaville. The internship begins in May/June 2026 and ends in August 2026. Potential interns must be able to commit to at least 40 hours per week throughout the summer. This internship is located at Lonza's production facility in Vacaville, California. The production facility makes pharmaceutical proteins from mammalian cells using large-scale production techniques. The Automation Lifecycle Management team supports all PLC based systems including VSC (vendor supplied controllers) for the entire Vacaville site. Additionally, the team supports projects for new products, equipment, and system upgrades across the site. We are seeking a motivated Intern to join our team. The successful candidate will have very strong communication skills, be self-motivated/driven and showcase problem solving mindset.

Requirements

  • Completion of junior year (typically 90 credits) towards a B.S. degree Chemical Engineering, Biomedical Engineering, Biological Sciences or a related field.
  • Minimum cumulative GPA of 3.0 (out of 4) required
  • Must currently be enrolled in BS or MS Academic Program
  • Proactive, detail-oriented team player with strong communication and collaborative problem-solving skills.
  • Self-motivation and the ability to contribute as a team member.
  • Ability to organize, plan and execute projects
  • Research skills and attention to detail

Responsibilities

  • Working with engineers and specialists to learn the science behind cell culture and purification unit operations of the manufacturing process.
  • Assisting in laboratory operations, including process buffer and chromatography column preparation, maintaining analytical equipment and monitoring of cell culture and purification step performance.
  • Completing lab-scale experiments for cell culture, chromatography, ultrafiltration/diafiltration and normal flow filtration operations.
  • Coordinating and participating in design and execution of process characterization and validation studies.
  • Documenting lab activities in electronic notebook, authoring test plan and technical reports, and presenting experiment outcomes in group meetings.
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