Our purpose
Our purpose is to bring hope to life by enabling life‑changing therapies for patients around the globe, creating a healthier and happier tomorrow.
Mission
Our mission is to work side by side with our customers in order to improve patients’ lives by bringing new biopharmaceuticals to market.
Responsibilities
* Support the planning of Automation & Q&M responsibility interventions.
* Support the preparation of Automation & Q&M responsibility documentation (SOP, Technical Report, Qualification Summary, etc.).
* Support the management of training for consultants/suppliers.
* Support the management of Change, Deviations and CAPA with impact on Automation & Q&M.
* Participate in regulatory inspections and client inspections.
Qualifications
* Knowledge of instrumentation used in laboratory and production environments.
* Familiarity with quality management processes, particularly the operational flows related to change control, deviation management and implementation of CAPA.
* Communication and relational skills to act as a strategic point of contact between internal users and external suppliers.
* Good knowledge of English.
Our culture
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.
About AGC Biologics
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 (WA), Boulder and Longmont (CO), Copenhagen (DK), Heidelberg (DE), Milan (IT), and Chiba (JP). 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 offers a highly competitive compensation package and a friendly, collaborative culture that values personal initiative and professional achievement.
EEO Statement
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.
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