*Technician for QC Bioassay, Quality Control

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Do you thrive in a dynamic environment with lots of exiting challenges every day? Do you want to be a part of a team of skilled colleagues and in an organization where we work as one team? QC Bioassay is looking for a Technician to join the team.

We are looking for a motivated colleague to join our QC Bioassay. As an employee in Quality Control at AGC Biologics in Søborg, you can look forward to a great deal of responsibility and 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 QC organization consists of six departments: QC Bioassay, QC Chemistry, QC Microbiology, QC Adjuvant, QC Stability and QC Raw Materials. QC is responsible for raw materials testing, the performance of analytical testing of batch release samples, planning and executing of stability programs and validation of analytical methods according to ICH guidelines.

Moreover, QC are responsible for supporting the ongoing manufacturing of biopharmaceuticals by testing of stop/go samples.

Role and Responsibilities

As a technician in QC Bioassay you will be involved in analytical testing of drug substance and drug product samples as well as in-process samples. Moreover, you will be involved in stability programs and validation of methods used for phase I/II and phase III/Commercial products.

Main responsibilities:

  • Execute a variety of Bioanalytical methods (e.g. ELISA, Endotoxin, SDS-PAGE, qPCR, Octet, Appearance, Solo, OD and Osmolality)
  • Report results including data processing in LIMS and setup
  • Participate in method validation studies
  • Participate in troubleshooting of methods
  • All testing is performed according the cGMP

Qualifications

The ideal candidate holds a degree as technician (laborant). We expect you to have a structured mindset, be able to work independently and meet tight deadlines with a can-do attitude but without compromising the quality.

In addition, we expect you to bring some of the following experience and characteristics:

  • Experience with performance of Bioanalytical methods
  • Experience working in a GMP environment
  • Good communication skills and a service-minded attitude as you will work closely with your stakeholders, mainly form the manufacturing
  • Has a flair for teamwork combined with the ability and desire to work independently
  • The ability to handle multiple tasks simultaneously in a busy environment
  • Fluent in written and spoken English

Application
Submit your application as soon as possible. We treat the applications as we receive then, and conduct interviews with qualified candidates. When the right candidates are found, the add will close.

For further information regarding the position, please contact QC Bioassay Manager Jona Uldall-Jessen, at +45 60253361 and Abdurrahman Sahan, at +45 27602468.

AGC offers
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.

For further information, please contact Jona Uldall-Jessen at [email protected]

For agencies, please contact our Talent Acquisition team at [email protected]

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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 "Laborant", og befinder sig i kategorien "Sundhed og forskning".

Arbejdsstedet er beliggende i København

Jobbet er oprettet på vores service den 7.4.2022, men kan have været deaktiveret og genaktiveret igen.

Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
  • Laborant
  • København

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