Do you want to be part of a company helping customers bring new advanced biological products to market? And do you thrive in a role where you learn and develop? Then these roles as a technician in our downstream team could be something for you.

AGC Biologics is a Contract Manufacturing Organization (CDMO) with facilities in Denmark, Germany, Japan and USA and with customers from all over the world. We have more than 35 nationalities employed and the daily language is English

The position
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.

As a Microbial downstream technician, you will work in a GMP environment with batch execution, batch documentation and optimization of purification process flows.  The Downstream unit operations runs on heavy machinery such as centrifuges and homogenizers, and you will be part of cleanings as well as filtration, TFF, chromatography and UNICORN bioprocesses.  In this role, you will work on the floor during production and be engaged securing batch readiness and release and you will take part in the maintenance of equipment.

Qualifications and experience
Our preferred candidate has the following profile:

  • Trained technician with hands-on experience preferably from recovery and/or purification.
  • +2 years of experience from a production environment within the 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 changing shifts 24/7, so you must be able to work flexible hours, both days, evening, nights and weekends.

AGC Biologics offers
AGC Biologics offers a dynamic working place with good opportunities for working with a varied array of tasks and challenges. This opens many doors for personal development and for you to make a real difference towards both patients and customer. At AGC Biologics the work environment is informal and humor is part of the work day. We respect each other and our differences, and we help each other to reach deadlines together as one team.

For more information please contact teamleader Helle Bidstrup Jensen at +45 2294 3015 0r Ruddi Vadt at +45 2760 2134

We will process the applications as they arrive. Therefore, please submit your application and CV as soon as possible. When the right candidates are found, the ad will close.

 

Want to keep posted about our growth and to learn more about our company?

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AGC Biologics (AGC) is a global Contract Development Manufacturing Organization (CDMO) with bio-manufacturing facilities in Europe, Japan, Italy and the USA. The company provides a comprehensive range of commercial and clinical cGMP biologics manufacturing services, from DNA to active pharmaceutical ingredient (API). The company’s team and approach are tailored to each of its client’s needs, whether turnkey manufacturing or sophisticated, stand-alone analytical, formulation and stability services.

 

Visit www.agcbio.com to learn why AGC Biologics is a World Leader in process development and contract manufacturing.

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