Principal Technician (Cover)

AGC Biologics A/S; København; Presencial; DKK 450.000 - 600.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Canteen arrangement

Employee Club

Employee discount opportunities

Descripción de la vacante

AGC Biologics A/S in Søborg, Denmark, is hiring a Principal Technician for mammalian upstream manufacturing. This fixed‑term maternity cover role combines hands‑on production with independent responsibility in a GMP environment.

Responsibilities include media preparation, aseptic handling, equipment setup (200–2,000 L), sampling, harvest, and GMP documentation. Fluency in English is required, and a strong reliability mindset is essential.

Formación

• Educational background in Process Operator, Process Technologist, Biotechnology Technician, or equivalent.
• 3–5 years of experience in GMP‑regulated manufacturing, preferably in biopharmaceutical production.
• Solid understanding of mammalian cell culture from thaw to harvest.
• Experience with upstream manufacturing equipment and GMP environments.
• Fluent in written and spoken English.

Responsabilidades

• Prepare media and aseptically handle mammalian cell cultures in a laminar airflow bench.
• Set up single‑use manufacturing equipment, including wave rockers and bioreactors (200 L–2,000 L).
• Perform daily sampling, feed additions, harvest, and clarification activities.
• Ensure GMP documentation and compliance with procedures and aseptic practices.
• Support troubleshooting, deviation investigations, and continuous improvement.
• Own training and share knowledge with colleagues as needed.

Educación

Process Operator / Process Technologist / Biotechnology Technician or equivalent

Descripción del empleo

Temp position – 12 Months | Expected Start: January 1, 2027 Are you an experienced upstream Principal Technician with a solid understanding of mammalian cell culture processes, from thaw to harvest? Do you enjoy taking responsibility for production activities while sharing your experience with colleagues? At AGC Biologics in Søborg, we are looking for a Principal Technician to join our Mammalian Upstream Manufacturing team for a nine-month maternity cover. You will become part of a team of eight, including your supervisor, working in a dynamic, GMP-regulated environment where different products and customer requirements call for technical understanding, adaptability, and attention to detail.

About the Job

As a Principal Technician, you will contribute to the execution of mammalian upstream manufacturing processes, ensuring that production activities are performed safely, efficiently, and in compliance with GMP requirements. The role combines hands‑on production work with independent responsibility, technical understanding, and close collaboration with your colleagues.

Your main responsibilities will include:

• Preparing media and performing aseptic handling of mammalian cell cultures in a laminar airflow (LAF) bench.
• Setting up single‑use manufacturing equipment, including wave rockers and bioreactors ranging from 200 L to 2,000 L.
• Performing daily sampling of cell cultures, feed additions, harvest, and clarification activities.
• Ensuring accurate and timely GMP documentation and compliance with approved procedures and aseptic practices.
• Supporting troubleshooting, deviation investigations, and continuous improvement activities.
• Taking ownership of your training and technical qualifications while sharing knowledge and providing practical guidance to colleagues when relevant.

Who Are We Looking For?

We imagine that you:

• Ideally have an educational background as a Process Operator, Process Technologist, Biotechnology Technician, or an equivalent relevant technical qualification.
• Have approximately 3–5 years of experience in GMP‑regulated manufacturing, preferably within biopharmaceutical production.
• Have a solid understanding of mammalian cell culture processes, from thaw to harvest.
• Have practical experience with upstream manufacturing equipment and processes, preferably in a GMP‑regulated biopharmaceutical environment.
• Are familiar with GMP requirements, aseptic practices, and accurate production documentation.
• Can independently execute manufacturing activities and contribute to solving operational challenges.
• Are fluent in written and spoken English.

Employment Period & Working Hours

This is a fixed‑term temp position for twelve months, with an expected start date of January 1, 2027, and an expected end date of December 31, 2027. The position follows a 5-2 day‑shift rotation, with working hours from 06:00–17:04.

What We Offer

We offer:

• The opportunity to work with mammalian upstream processes and different manufacturing setups, applying and developing your technical expertise.
• A role where your experience matters, both in daily production and in supporting your colleagues.
• A supportive and approachable manager who values quality, accountability, and open communication.
• A close-knit team where knowledge sharing, collaboration, and continuous improvement are encouraged.
• Access to our canteen arrangement, Employee Club, and employee discount opportunities.

Who We Are

AGC Biologics is a global Contract Development and Manufacturing Organization with a strong presence in Denmark. From our Søborg site, we develop and manufacture life‑changing advanced biologics for some of the world’s most innovative pharmaceutical companies. Together with our team members across Europe, the U.S., and Japan, we deliver development and manufacturing of mammalian and microbial‑based therapeutic proteins, plasmid DNA (pDNA), messenger RNA (mRNA), viral vectors, and genetically engineered cells therapies. Across our global network, we are united by one mission: To work side by side with our customers in order to improve patients’ lives by bringing new biopharmaceuticals to market. AGC Biologics is Your Friendly CDMO Expert – dedicated partners with the expertise and commitment to support our customers and teams. We work with some of the world’s most innovative pharmaceutical companies to develop and manufacture their life‑changing drug products. If you’re motivated by meaningful impact and ready to join our journey, we invite you to explore our current opportunities!