12 Months Temporary HPLC Scientist for QC Chemistry

Are you looking for an exciting job in an international and challenging environment? Do you thrive in a dynamic environment, in a department with skilled colleagues in an organization where we work as one team? This is a great opportunity to make the most of your expertise and passion for analytical chemistry.

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.

The Department

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.

Roles and responsibilities

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 authoring SOPs.

Your Profile

The ideal candidate holds a MSc or PhD degree in Biochemistry, Chemistry or relevant area and has some 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 Fluent in written and spoken English 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.

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 ad will close.

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