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.
At AGC Biologics in Søborg, your work in buffer preparation plays a critical role in ensuring that biologic medicines can be produced safely and consistently for patients worldwide.
You will join SYD22, a new, state-of-the-art facility currently ramping up production across preclinical, clinical, and commercial products. This is a unique opportunity to become part of a growing environment where your contributions help shape both processes and team ways of working from the ground up.
The team consists of highly skilled technicians and academics who operate with a high level of professionalism and collaborate closely with key partners, including QA, QC, PLE, PE, and Manufacturing Product Support.
As a Technician in Buffer Preparation, you will be responsible for planning and executing different buffers used in the protein purification production process in a cGMP-regulated environment.
Your Work Will Include
What We Offer
About You
You likely have experience from a GMP-regulated production environment and enjoy working in a structured yet fast-paced setting where reliability and precision matter.
To succeed in this role, you bring:
As a person, you are positive, flexible, and motivated by taking on new assignments and responsibilities. You thrive in a dynamic production environment and are able to handle change and unpredictability.
The position is shift-based according to a defined shift plan. Production operates 24/7, including weekends and holidays, and you will be expected to work during these periods depending on your assigned shifts.
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 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.