Are you looking for an exciting job in a multicultural, international and never boring environment? Do you thrive in a challenging and fast pace work environment, taking on an active role 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 knowledge, sharing your 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.
Your role and responsibilities
As scientist in QC Chemistry it is required that, you have proven expertise and ability to troubleshoot on chromatographic methods, especially (U) HPLC, iCIEF and CGE-SDS.

You will be reviewing, releasing and conducting stability analyzes, supporting the lab technicians on a daily basis. Part of your daily focus is documenting validation activities of analytical methods for clinical phase I/II and III and authorizing SOPs.

You will represent QC Chemistry in customer project teams, and good communication skills are essential when managing stakeholder expectations, together with proven projects management experience.

Your profile
The ideal candidate holds a MSc or PhD degree in Biochemistry, Chemistry or relevant area and has minimum 5 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
  • Interest in and experience in project management acting as QC representative in customer projects
  • Fluent in English (both written and verbal)
  • Experience with working in cGMP settings according to European and US regulatory guidelines

It is crucial that you 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.

For further information, please contact Palle Rasmussen at 
For agencies, please contact our Talent Acquisition team at

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

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