Intern, Engineering

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

Key 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.

Qualifications

• 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 understanding of biologics manufacturing unit operations is a plus.

• 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.

Our culture at AGC Biologics is defined by the six core values: Knowledge Trust Quality Ingenuity Accountability and Teamwork. Our core values stem from our team members and are embedded into our DNA. They provide a common language and understanding of how we as an organization are connected across three continents. Our core values serve as a compass and reminder of how we achieve our purpose of bringing hope to life for patients around the globe.

AGC Biologics is a leading global biopharmaceutical Contract Development and Manufacturing Organization (CDMO) with a strong commitment to delivering the highest standard of service as we work side-by-side with our clients and partners every step of the way. We provide world-class development and manufacture of mammalian and microbial-based therapeutic proteins plasmid DNA (pDNA) messenger RNA (mRNA) viral vectors and genetically engineered cells. Our global network spans the U.S. Europe and Asia with cGMP-compliant facilities in Seattle Washington; Boulder and Longmont Colorado; Copenhagen Denmark; Heidelberg Germany; Milan Italy; and Chiba Japan. We currently employ more than 2500 employees worldwide. Our commitment to continuous innovation fosters the technical creativity to solve our clients most complex challenges including specialization in fast-track projects and rare diseases. AGC Biologics is the partner of choice. To learn more visit.Want to keep posted about our growth and learn more about our company Follow us on LinkedIn and give us a quick Like on Facebook!

AGC Biologics offers a highly competitive compensation package and a friendly collaborative culture that values personal initiative and professional achievement. AGC Biologics is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age ancestry color family or medical care leave gender identity or expression genetic information marital status medical condition national origin physical or mental disability political affiliation protected veteran status race religion sexual orientation or any other characteristic protected by applicable laws regulations and ordinances.