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Experienced Scientist for QC Chemistry

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 scientist in QC Chemistry and be part of a growing global CDMO

 

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. QC Chemistry is responsible for supporting the production of new biopharmaceuticals by performing analytical testing and validating various analytical procedures according to ICH guidelines from clinical phase I to phase III and commercial. QC Chemistry have a close collaboration within the QC area and with departments across the organization.

 As scientist in QC Chemistry it is required that you have expertise and ability to troubleshoot on chromatographic methods, especially (U)HPLC, iCIEF and CGE-SDS. You will be reviewing release and stability analyzes, supporting lab technicians on a daily basis, documenting validation activities of analytical methods for clinical phase I/II and III and authoring SOPs. You will represent QC Chemistry in customer project teams, and good communication skills are essential.  

Your Profile

The ideal candidate holds a MSc or PhD degree in Biochemistry, Chemistry or relevant area and has several years of work experience in analytical development or quality control. In addition, we expect you to bring some of the following experience and characteristics: 

  • Working and troubleshooting experience with SE-, IEX- and RP-UHPLC, iCIEF and CGE-SDS analysis.
  • Experience with writing SOPs and method validation documentation
  • Experience with Chromeleon software and LIMS
  • Technical experience in protein analytics testing and protein biochemistry
  • You like to share your knowledge and communicate openly and professionally both internally and with external customers
  • You are able to prioritize your own tasks in a dynamic environment
  • You are a team player, but work independently
  • Excellent communication, presentation and interpersonal skills
  • Experience with working in cGMP settings according to European and US regulatory guidelines

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. We will process the candidates as they arrive. Therefore, please submit your application and CV as soon as possible. When the right candidates are found, the add will close. We are therefore looking forward to receive your application today! 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 CMC Biologics’ innovative approach to cell line and process development.

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


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