Bemærk at denne jobannonce er udløbet!
Annoncen er udløbet, og stillingen kan ikke længere søges. Opslaget vises udelukkende som reference

Scientist for QC Bioassay, Temporary Position

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? QC Bioassay is looking for a Scientist to a temporary position. The DepartmentQC Bioassay is part of the QC organization which consists of six departments: QC Bioassay, QC Chemistry, QC Microbiology, QC Adjuvant, QC Stability and QC Raw Materials. QC are responsible for supporting production of new biopharmaceuticals by controlling raw materials, performing analytical testing, planning and executing stability programs and validating various analytical methods according to ICH guidelines from clinical phase I to phase III and commercial. Role and ResponsibilitiesAs a Scientist in QC Bioassay you will be involved in a range of exciting tasks and challenges. Your main responsibility area will be review and approval of analytical setups, thus delivery of scientifically sound and cGMP compliant analytical results. All work are done within deadline in close collaboration with your colleagues. Responsibility areas:

  • Review and approval of analytical setups
  • Drive Initial Laboratory Investigations and deviations related to QC activities
  • Troubleshooting and scientific support on selected bioassay method
  • Ensuring all tasks performed in cGMP compliance.

 QualificationsThe ideal candidate holds a master degree within life sciences and a few years of work experience within the pharmaceutical industry preferable working in an analytical development or quality control area. In addition, we expect you to bring some of the following experience and characteristics: 

  • Experience, theoretical and hands-on, with bioanalytical methods e.g. ELISA, LAL, and methods for measurement of protein concentration
  • Good analytical and troubleshooting skills
  • Experience working in a GMP environment and knowledge of relevant guidelines
  • Good communication skills and a service-minded attitude to meet customer requests in a positive and professional way
  • The ability to handle multiple tasks simultaneously in a busy environment
  • Fluent in written and spoken English.

 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.


Mere af samme slags?

Modtag jobannoncer der minder om dette job i din indbakke.




Når du tilmelder dig accepterer du samtidig vores privatlivspolitik. Du kan altid trække dit samtykke tilbage.

Mere af samme slags?

Modtag jobannoncer der minder om dette job i din indbakke.




Når du tilmelder dig accepterer du samtidig vores privatlivspolitik. Du kan altid trække dit samtykke tilbage.