Intern, Engineering

AGC BiologicsBothell, WA
7d$27Onsite

About The Position

Our purpose is to bring hope to life by enabling life-changing therapies for patients around the globe, creating a healthier and happier tomorrow. Our mission is to work side by side with our customers in order to improve patients’ lives by bringing new biopharmaceuticals to market. Job Summary We are looking for an Intern/Co-op to join our Engineering teams to support technology transfer, validation, and continuous improvement initiatives that enable GMP manufacturing operations. This role offers hands-on exposure to real-world engineering projects in a regulated biopharmaceutical environment and provides opportunities to collaborate across Manufacturing, Process Development, MSAT, and Quality teams. This is an excellent opportunity for a motivated student to gain practical experience, develop technical and professional skills, and contribute to projects that improve manufacturing reliability and performance. Location : Bothell, WA Schedule : 3 or 6 months. Starting in May or June 2026 Compensation : $27 per hour

Requirements

  • Currently pursuing a degree in engineering or a related scientific discipline.
  • Completion of at least two years of undergraduate coursework.
  • Coursework or interest in areas such as process control, bioprocess design, bioreactors, bioseparations, or statistical data analysis.
  • Basic knowledge of cGMP principles.
  • Strong organizational skills and ability to manage multiple tasks.
  • Clear written and verbal communication skills.
  • Strong technical writing and data presentation skills.
  • Self-motivated, proactive, and comfortable working in a team-based environment.

Nice To Haves

  • Basic understanding of biologics manufacturing unit operations is a plus.

Responsibilities

  • Support engineering-led projects focused on manufacturing reliability, documentation workflows, and data analysis.
  • Assist Staff Engineers on cross-functional project teams to meet project deliverables.
  • Support validation activities, including drafting, reviewing, and executing validation documentation and studies.
  • Interface with vendors to help define scope, obtain quotes, and support project timelines.
  • Assist with capital project documentation, including business cases and justification materials.
  • Perform data analysis related to equipment reliability, asset lifecycle, and automation improvements.
  • Develop documented recommendations for continuous improvement, future investments, and cost savings.
  • Collaborate with Manufacturing, Process Development, MSAT, and Quality teams to support process control and operational improvements.
  • Support response to on-floor manufacturing issues as needed.
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