*QC Laboratory Technician for Cell-based assay
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The Department
The QC organization consists of five departments: QC Bioassay, QC Chemistry, QC Microbiology, QC support and QC planning & systems. QC are responsible for release testing of clinical and commercial batches, and validation of the analytical methods, as well as analysis of raw materials and stability programs. We are working in an international and customer oriented way to secure fast and reliable manufacturing of medicines to our customers.
The current position in located in QC Bioassay in the Cell and Reference material group, in Søborg, Denmark. QC Bioassay Cell and Reference material is one of four departments in the QC Bioassay area. QC Bioassay Cell and Reference material is responsible for supporting the production of new biopharmaceuticals by performing analytical testing and validating various analytical procedures according to ICH guidelines and regulatory bodies from early phase to commercial. QC Bioassay Cell and Reference material have a close collaboration within the QC area and with department across the organization.
Roles and responsibilities
As a Cell-based assay technician you will be a part of a dedicated team with highly competent colleagues focusing on Cell-based assays. You will be involved in multi-disciplinary projects working in close collaboration with team members and/or in project groups across the QC Bioassay Cell based assays groups responsibilities.
The main tasks will be the following:
- Routine maintenance of cell lines
- Testing of release and stability samples in cell-based assays
- Validation of cell-based assays
- Daily housekeeping of cell laboratory
- Documentation according to our quality system GDP/GLP/GMP
- Responsible for analytical equipment i.e. keeping log books, ensure service has been performed etc.
- Working according to cGMP
- Be able to utilize new knowledge quickly and have good communication skills
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.
Your profile
The ideal candidate holds a degree as technician (laborant) or equivalent, and has a minimum of 3-5 years of work experience in analytical development or quality control. 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 bring some of the following experience and characteristics:
- Experience within Cell-based assays
- Experience working in a Cell laboratory
- Experience working in a GMP environment
- Good communication skills and a service-minded attitude as you will work closely with different stakeholders
- The ability to handle multiple tasks simultaneously in a busy environment
- Fluent in written and spoken English
Join an international and agile organization
At AGC, you will get great opportunities to work with a wide array of tasks and challenges, and you will get experience with our various departments. Furthermore, as we plan projects and tasks together in the team, you will get the opportunity to influence your daily work. AGC offers an informal working environment where high energy and enthusiasm is part of the daily work life. We respect each other and our individual differences. At AGC, we have a flexible attitude, and we help each other reach deadlines as a team.
Contact and application
For any further questions, you are more than welcome to contact Manager Anne Lykkegaard Widlund phone 27602154 or email: [email protected]. Please be aware that we take in consideration only the applications send via our career page and, not via email. We will process the applications as they arrive.
Want to keep posted about our growth and to learn more about our company?
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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 14.11.2023, men kan have været deaktiveret og genaktiveret igen.
- Laborant
- København
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