Join to apply for the GMP Downstream Technician role 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 to improve patients' lives by bringing new biopharmaceuticals to market.
Main Activities Purification of viral vectors using chromatographic and tangential ultrafiltration systems following standard operating procedures and completing GMP documentation, batch records, and forms; Setup of equipment and materials necessary for processing; Preparation of solutions in GMP areas for purification processes; Execution of minor routine maintenance and periodic calibration of equipment; Work under laminar flow hood: sampling, fluid transfers, filtration of solutions and bulk materials to be purified or purified; Preparation of GMP manufacturing documentation: Batch Records, SOPs, protocols, and reports; Management of documentation related to change controls and deviations. Requirements Degree in Biotechnology or related field; Previous experience with the above techniques; Preferred experience in controlled environments (Cleanroom) and familiarity with GMP. Our culture at AGC Biologics is defined by six core values: Knowledge, Trust, Quality, Ingenuity, Accountability, and Teamwork.
These values are embedded into our DNA and guide how we work across continents to fulfill our purpose of bringing hope to life for patients globally.
AGC Biologics is a leading global biopharmaceutical CDMO, committed to delivering high-quality services.
We develop and manufacture therapeutic proteins, plasmid DNA, mRNA, viral vectors, and engineered cells across our facilities in the U.S., Europe, and Asia, employing over 2,500 employees worldwide.
We foster innovation and specialize in fast-track projects and rare diseases.
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We offer a competitive compensation package and a collaborative culture valuing initiative and achievement.
We are an equal opportunity employer, considering all qualified applicants without discrimination based on legally protected characteristics.
Seniority level Entry level Employment type Full-time Job function Management and Manufacturing Industries Pharmaceutical Manufacturing
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