AGC Biologics is a leading global Contract Development and Manufacturing Organization, with a deep commitment to improving life quality by bringing new biopharmaceuticals to market. Because of our dedication to building and empowering our internal teams, AGC Biologics is an innovative leader in the industry with an extensive network of cGMP facilities in the US, Europe and Asia. As such, we deliver a deep expertise, dynamic solutions and technologies, as well as customized services for the scale-up and cGMP manufacturing of protein-based therapeutics. We forge exceptionally strong partnerships with our clients, and we never lose sight of our pledge to deliver a reliable and compliant drug substance supply. Right. On time. For more information, visit www.agcbio.com.

AGC Biologics is in continuous growth and we are currently looking for new colleagues to join us in Manufacturing. If you would like to work hands-on with a wide variety of different biopharmaceutical production processes, innovative technologies and state-of-the-art facilities, these positions will definitely be something for you.

The positions
You will become part of our manufacturing area consisting of five production lines, which produce pre-clinical, clinical and commercial products for a wide variety of different customers coming from around the world. You will be part of a group of highly dedicated technicians and scientists working with various stakeholders such as QA, QC and Development.

You will work in a dynamic GMP environment with batch execution, batch documentation and optimization of purification process flows. Downstream unit operations ranges from centrifugation, homogenization, filtration, TFF, chromatography and UNICORN bioprocesses. In this role you will work on the shop floor during production and be engaged securing batch readiness and release and you will take part in the maintenance of equipment.

As we employ state of the art technologies both within upstream- and downstream production, your preferred individual development path is huge.

Qualifications and experience
Our preferred candidate has the following profile:
• Trained technician with hands-on experience preferably from purification.
• +2 years of experience within Biopharmaceutical industry.
• Experience working in a cGMP environment
• Experience with process optimization (LEAN)
• Interest in maintenance of equipment
• Excellent collaboration- and communication skills
• Ability to speak and write in English

As a person, you have a positive mind, are flexible and enjoys taking on new tasks and responsibilities. You thrive in a dynamic environment and can cope with uncertainties.

Our manufacturing teams are working in shifts during production so you must be able to work outside normal work hours.

For more information please contact Teamleader Helle Bidstrup Jensen at 2294 3015 or Teamleader Markus Jondelius Hederos at 2080 6095.

We will process the applications as they arrive. Therefore, please submit your application and CV as soon as possible and no later than September 1st, 2019.

About us
Currently, AGC Biologics employs more than 900 people worldwide with 320 employees situated at our Søborg site close to Copenhagen, Denmark. The site occupies employees from more than 30 different countries around the world and therefore you will be part of an exciting organization with high diversity. We have an informal and humorous working environment, where we respect each other and our differences. AGC Biologics employees are flexible and take pride in working together to achieve goals - as one team.