*Experienced Technician for Analytical Development
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We are looking for an experienced technician for a permanent 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 really good team in an open and informal environment with solid professionalism, high pace and lots of 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). These groups are responsible for implementing analytical methods, supporting the Upstream and Downstream Process Development and engineering batches from Manufacturing with analytical results, as well as conducting AD studies e.g. non-GMP stability, in use stability, forced degradation etc.
Within this broad field of responsibilities, with many different customers’ projects and with various biopharmaceuticals, the AD department differs from traditional AD lab. AD has a close collaboration with customers, and departments across the organization to provide data demonstrating the level of control in all steps in a manufacturing process.
Role and Responsibilities
- Execute a variety of methods within Bioassay e.g. ELISA, Octet, qPCR, SDS-PAGE
- Report results including data processing
- Documentation according to our quality system GDP/GLP/GMP
- Implementation of new methods in close collaboration with a scientist
- Participate in transfer of methods from AD to QC
- Responsible for analytical equipment i.e. keeping log books, ensure service has been performed etc.
- Collaborate across departments
- Participate in troubleshooting of methods
Qualifications
In our new colleague, we are looking for a person with an education as a laboratory technician or similar, combined with practical experience in execution of the methods below.
- 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 GDP/GLP/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
- Writes and speaks English at a high level
About AGC Biologics
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.
Application
Please apply online by uploading your application and CV. We are screening for candidates on an ongoing basis, so do not hesitate to enter your submission. If you have further questions, please contact Mette Blem Skydtsgaard, Bioassay Team leader, Analytical Development, phone +45 2265 6903 or Helle Grann Wendelboe, Senior Director of Analytical Development, phone +45 2294 3090.
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 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.
Information og data
Denne ledige stilling har jobtypen "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i København
Jobbet er oprettet på vores service den 5.9.2023, men kan have været deaktiveret og genaktiveret igen.
- Øvrige
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