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Temporary Technician (Laborant) for QC Chemistry, HPLC/Chromatographic Analysis

Do you thrive in a dynamic environment, in a department with skilled colleagues in an organization where we work as one team? If yes – you may want to join our department as temporary technician (6 months) in QC Chemistry and be part of a growing global CDMO!

QC Chemistry at AGC Biologics A/S is expanding and looking for a temporary technician for HPLC/Chromatographic analysis to support manufacturing and stability studies.


The job

At AGC Biologics A/S (AGC), 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 Chemistry is one of five 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 temporary technician in QC Chemistry, you will be responsible for performing HPLC analysis such as RP-UHPLC, SE-UHPLC, HIC-UHPLC, cIEX-UHPLC, CE-SDS, peptide mapping and iCIEF.

The position requires experience within HPLC/Chromatographic analysis. QC Chemistry performs analyzes for manufacturing and stability studies of the API and validation of analytical methods for clinical phase I/II and III. All work is performed under cGMP. You will be responsible for equipment in QC and should help to ensure that existing procedures and guidelines are followed.


Your Profile

We expect you to hold a degree as laboratory technician or similar and bring several years of work experience within analytical development or quality control as a laboratory technician. In addition, we expect you to have:

  • Technical experience in (U)HPLC analysis, iCIEF and/or CE-SDS
  • 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

Applicants with practical experience in HPLC, iCIEF and/or CE-SDS analysis will be preferred.

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.


AGC offers
AGC offers a dynamic working place with good opportunities of working with a varied array of tasks and challenges. You will get insight into and experience with the way the various departments throughout a contract manufacturing organization interact in order to achieve success. Exciting and challenging assignments will constantly come your way, and you will to a large extend be able to plan your daily work yourself. AGC offers an informal working environment, where humor is part of the daily work life. We respect each other and our individual differences. AGC’s employees have a flexible attitude and we help each other to reach deadlines together as one team. ?ApplicationWe continuously evaluate incoming applications and conduct interviews accordingly. Therefore, please submit your application and CV as soon as possible. When the right candidates are found, the ad will close.

For further information about the position, please contact Team Lead Nina Lei, telephone +45 2269 9363, or Sr. Manager Eva Andersen, telephone +45 2760 2094.


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 to learn why AGC Biologics is a World Leader in process development and contract manufacturing.

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