Technician for QC Chemistry, HPLC/Chromatographic analysis

  • Job reference

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 might be our new technician in QC Chemistry and be part of a growing global CDMO! 

QC Chemistry at AGC Biologics A/S is expanding and looking for a 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 & Responsibilities
As 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. 

How to apply
Interested? Upload CV, motivation letter, references and criminal record via the link on this page, and do it as soon as possible. AGC Biologiscs is partnering with Adecco on this recruitment, so if you have any questions about the position, you can contact our recruitment team: 

Line Heyn +45 5185 7005
Christina Drejet +45 3838 7007 

About AGC Biologics 
AGC Biologics (AGC) is a global Contract Manufacturing Organization (CMO) with biomanufacturing facilities in Europe, Japan 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.  
AGC Biologics also offers non-exclusive license to CHEF1™, a proprietary CHO cell line development platform. CHEF1 delivers stable, high-titer, production-quality cell lines in optimized time frames. It is the foundation of AGC Biologics’ innovative approach to cell line and process development.  
Visit to learn why AGC Biologics is a World Leader in process development and contract manufacturing.  


Andre oplysninger

Om AGC Biologics

Adecco Recruitment
+45 5185 7005 /+45 3838 7007