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The Job
AGC is growing - we are building a new facility next to our existing facility in Søborg. To support the existing laboratory equipment as well as the expansion of the laboratory we are looking for a technician, 6 months in a temporary position, to support QC Bioassay with tasks related to qualification and maintenance of equipment intended for GMP use.
At AGC Biologics A/S, we work with the development of biopharmaceutical manufacturing processes and GMP manufacturing of biopharmaceutical proteins for both clinical testing and marketing. Since we are a contract manufacturing organization, a high level of service to our clients is in focus. QC Bioassay is one of six departments in the QC area, where we are responsible for supporting the production of new biopharmaceuticals by performing analytical testing of samples from the production and stability programs and validating various analytical procedures according to ICH guidelines from clinical phase I/II to phase III and commercial. Within this broad working area and with various biopharmaceuticals, the QC area have a close collaboration with all departments across the organization.
Tasks and Responsibilities
As instrument technician in QC Bioassay, you will be responsible for ensuring analytical instruments related to bioassay methods; this includes ELISA, LAL readers, SoloVPE, qPCR, instruments etc.
The position requires hands-on experience with instrument maintenance. All work in the department is performed under cGMP and you will be responsible for performing the maintenance experiments, finalizing service reports and enter work performed in the equipment database.
You will be part of our QC Bioassay Instrument team and together you will be responsible for completion of all qualifications and maintenance activities within deadlines.
Your Profile
We expect you are a trained technician or similar background preferably with knowledge on instrument qualification and maintenance from the pharmaceutical industry.
In addition, we expect you to have:
- Technical understanding of instruments related to bioanalytical methods (e.g. ELISA readers, qPCR instruments, SoloVPE, LAF-benches)
- Experience with working in cGMP settings according to European and US regulatory guidelines
- Good communication and interpersonal skills
- Ability to interact positively within a team and in close collaboration with other working areas when needed
It is important to have a self-motivating personality with a pragmatic attitude and approach to the daily work - without compromising quality. Furthermore, you thrive in a challenging and dynamic environment and enjoy a rapid pace of work. You bring a positive, can-do attitude and a good sense of humor.
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 Manager Anne Widlund, QC Bioassay, at +45 2760 2154.
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 Anne Lykkegaard Widlund 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 "Øvrige", og befinder sig i kategorien "Øvrige stillinger".
Arbejdsstedet er beliggende i København
Jobbet er oprettet på vores service den 28.3.2022, men kan have været deaktiveret og genaktiveret igen.
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- København
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