*Temporary Technician for QC Stability
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The Department
QC Stability is part of the QC organization, which consists of several departments: QC Bioassay, QC Chemistry, QC Microbiology & QC Support.
QC Support consists of three departments; QC Stability, QC Samples & Service & QC Raw materials.
The QC area is responsible for supporting the production of various biopharmaceuticals by controlling raw materials, performing analytical testing, planning and executing stability programs and validating analytical methods according to regulatory guidelines from clinical phase I/II to phase III and commercial.
QC Stability is responsible for conducting our customer’s stability programs for Drug Substances as well as Drug Products. Furthermore, QC Stability also conducts annual testing of reference materials on request and offers support in freeze-thaw cycle studies of the biopharmaceuticals on request.
We are currently looking for a new colleague to join our QC Stability team, which consists of 8 skilled colleagues; five scientists and three technicians.
Tasks and Responsibilities
As a laboratory technician (laborant) in QC Stability, you will take part in the responsibility of keeping the overview of pulls of stability samples according to the protocols for the stability studies, including
- maintenance of the equipment used for the stability studies;
- ordering and packing of shipments for stability samples for external laboratories;
- collect analytical results for the stability samples from internal/external laboratories.
In addition, you will together with the rest of the team ensure that we are working according to cGMP compliance in everything we do.
Your profile
The ideal candidate is laboratory technician (laborant) by education and with work experience within the pharmaceutical industry preferably working in a quality control area.
You are motivated by working with documentation, spreadsheets and ensuring traceability. As a person, you thrive equally with being in the laboratory and working at your office desk.
In addition, it is advantage if you to bring one or more of the following experience and characteristics:
- Experience with stability programs of drug substances and/or drug products
- Good communication and interpersonal skills as well as a service-minded attitude
- Knowledge of cGMP systems according to European and US regulatory guidelines is an advantage
- Interest in and the ability to identify areas of improvements to optimize the flow of tasks
- The ability to handle multiple tasks simultaneously in a busy environment
- A ‘can-do’ attitude and a good sense of humor
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. 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
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 ad will close.
For further information, please contact Gitte Damgaard at [email protected] or Gulcan Yilmaz at [email protected]
For agencies, please contact our Talent Acquisition team at [email protected]
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 12.12.2022, men kan have været deaktiveret og genaktiveret igen.
- Øvrige
- København
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