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Experienced technician for Analytical Development

Do you enjoy speeding up in the laboratory and doing your own data processing, then you might be the one we are missing in our team!
We are looking for an experienced technician for a 14 months temporary position in Analytical Development, Bioassay. As an employee in the development department at AGC Biologics in Søborg, you can look forward to a great deal of responsibility and very varied work tasks. You can also look forward to being part of a great team in an open and informal environment with solid professionalism, high pace and many good laughs.
The Department
The AD department at AGC Biologics consists of four teams: AD PD support (9), AD HPLC (9), AD Bioassay (8) and AD Characterization (6). The AD groups are responsible for implementing of analytical methods, supporting the Upstream, Downstream Process Development, and Production for engineering batches with analytical results and conduct AD studies e.g. non-GMP stability, in use stability, forced degradation etc.
Within this broad working area, with many different customers’ projects and with various biopharmaceuticals, the AD department differs from traditional AD lab. 
AD have a close collaboration with customers, and departments across the organization to control all steps in the manufacturing processes.
Role and Responsibilities 

  • Perform a variety of methods within Bioassay ex. ELISA, Octet, qPCR, SDS-PAGE.
  • Report results including data processing
  • Documentation according to our quality system
  • Participate in transfer of methods from AD to QC
  • Responsible for analytical equipment i.e. Keeping log book, ensure service has been performed etc.
  • Collaborates across departments
  • Participate in troubleshooting of methods

Qualifications
You have an education as a laboratory technician or similar, combined with practical experience in performing ELISA and gel-based methods.

In our new colleague, we are looking for a person with: 

  • Experience with development and execution of analytical methods within Bioassays ex. ELISA, Octet, qPCR, SDS-Page
  •  Experience with equipment responsibility combined with a desire to help solve technical problems
  • Good documentation practice required and experience with GMP will be an advantage
  • Likes both development tasks and routine tasks
  • Thrives on working at a high pace in a busy company with varying tasks
  • Has a flair for teamwork combined with the ability and desire to work independently
  • Fluently in English both spoken and written.

 If you would say that the above description matches your profile, we would love to hear from you. We hope to find our new colleague as soon as possible, so please do not hesitate and send your application today. We will review the applicants on an ongoing basis. If we find the right candidate quickly, the job add will close.

A formal start date is preferred on January 1st 2021 at the latest. This position will be based in Denmark at our Søborg site.

Want to keep posted about our growth and to learn more about our company?
We also urge you to follow us on our LinkedIn Company Page and give us a quick Like on Facebook !

AGC Biologics (AGC) is a global Contract Manufacturing Organization (CMO) 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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