Description de l’offre d’emploi

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 III and authoring SOPs. You will represent QC Chemistry in customer project teams, and good communication skills are essential together with projects management skills.

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.

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

Exigences professionnelles

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 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.

Informations détaillées relatives à ce poste
Secteur:
Professional, scientific and technical activities
Secteur professionnel:
Life science professionals
Domaine d’enseignement:
Life sciences
Work experience:
Work experience is not required
Compétences linguistiques:
  • English
  • Good
Fourchette salariale:
Not provided
Date of expiry:
Link for more information:
QC HPLC Scientist

À propos de l’entreprise

The Danish job market is booming and many sectors are facing skills shortages. Therefore, there are many sectors with good job opportunities one of them is Life Science. The Danish life sciences industry, comprising almost 1.500 life sciences companies and approximately 47.300 employees, contribute considerably to both R&D, economic progress and employment in Denmark. Subsidiaries of… Pour en savoir plus