Student Assistant, Quality

at  AGC Biologics

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.
Student Assistant for Quality Control
The QC Department seeks a student assistant to support AGC Biologics in our continuous growth. You will become part of a QC student group that works closely with technicians and scientists in all QC departments managing many different tasks.
Do you see yourself contributing to our continuous growth?
Then join AGC Biologics in a QC student role and become part of an international and modern organization that delivers biopharmaceutical development and manufacturing.
Key Responsibilities
As a Student Assistant in our QC Department, you will be part of our new surveillance team in the QC Department. You will work closely with the other QC students, technicians, and scientists throughout the QC to assist them in several tasks.
Furthermore, you will get great insight into the biopharmaceutical industry.

The QC Department has a positive and proactive profile that is committed, professional, and with a friendly collaboration. You will be helping our QC Department with tasks including:

• Daily surveillance of our FMS and wFMS systems from Monday to Friday.
• Maintain equipment.
• Prepare documents for re-qualification of equipment.
• Scan and archive GMP documents.
• Support the QC Department with ad hoc tasks.

The QC surveillance team will be a team of three QC Students covering equipment surveillance from Monday to Friday, between 08 AM and 04 PM. You will be able to plan your work hours internally in the team.
About you
You are easy-going, detail-oriented, service-minded, and driven by the opportunity to learn the biopharmaceutical industry by doing relatively essential yet straightforward supportive tasks for our teams.
You have a positive can-do attitude and have the personal resources to master a job with working hours in a fast-paced company on top of your studies.
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 2,500 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 www.agcbio.com. Want to keep posted about our growth and learn more about our company? Follow us on
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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

• Daily surveillance of our FMS and wFMS systems from Monday to Friday.
• Maintain equipment.
• Prepare documents for re-qualification of equipment.
• Scan and archive GMP documents.
• Support the QC Department with ad hoc tasks