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Downstream Process Transfer Scientist

A challenging and varied job in our Process Transfer Department in Copenhagen is open for a quality-minded new colleague with downstream processing experience and a strong ability to drive interdepartmental collaboration.


The Job

AGC Biologics continues to enjoy great success, with a steadily increasing number of projects – many of which are late stage development projects preparing for commercial launch. At the same time, we are handling many new and exciting customer projects and give support to processes already running in our GMP facility for clinical and commercial supply. With AGC Biologic´s increasing activities, we are looking for a new colleague within downstream process transfer.

Depending on your level of qualification, you will take part in key downstream process activities in several projects, both within microbial and mammalian processing. As a Process Transfer Scientist, you will be responsible for:

  • Process transfers from customers and development into our manufacturing area
  • Process dimensioning and evaluation
  • Support to GMP downstream manufacturing processes

The position offers interaction with a large number of stakeholders, and is unique in having contact with both our customers and internal departments involved in process development, manufacturing and quality. You will be introduced to biopharmaceutical companies from all over the world and be an active player in their projects.


The Department

The Process Transfer department currently consists of 3 teams (Upstream Process Transfer, Downstream Process Transfer and Process Validation) and you will be part of the Downstream Process Transfer Team which includes 6 scientists and a Team Leader. We have an open communication and strong support and flexibility within the team and between the department teams.


Your profile

Our new colleague should have the following experiences:

  • D. or M.Sc. within biochemistry, protein chemistry, biotechnology, or similar educational background.
  • A few years of experience within biopharmaceutical development and/or manufacturing
  • Experience and knowledge of biopharmaceutical downstream unit operations.
  • Excellent English communication and collaborative skills
  • A flexible approach and desire to take on and drive new tasks and responsibilities
  • Strong driver of interdepartmental tasks with the ability to prioritize between many different tasks

 AGC Biologics Copenhagen
AGC Biologics offers a dynamic working place and an excellent opportunity for working and growing with a varied array of tasks and challenges. You will get insight into and experience with the way the various departments throughout a biologics contract development and manufacturing organization interact in order to achieve success. Exciting and challenging assignments will keep coming your way, but you will to a large extent be able to plan your daily work on your own. AGC Biologics offers an informal working environment, where humor is part of the daily work life. We respect each other and our individual differences. AGC employees have a flexible attitude and we help each other to reach deadlines together as one team, in accordance with our slogan - Right. On Time.



We continuously evaluate incoming applications and conduct interviews accordingly. Therefore, please submit your application and CV as soon as possible. When the right candidate are found, the ad will close. 


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

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