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Equipment Technician (udstyrslaborant) for QC Chemistry, UHPLC, CE-SDS and iCIEF

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 (UHPLC) equipment technician in QC Chemistry and be part of a growing global CDMO! QC Chemistry at AGC Biologics A/S is expanding and looking for a technician to maintain and repair UHPLC/Chromatographic equipment to ensure that equipment is in service at all time to support analyses for manufacturing and stability studies.  The JobAt 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, where we are responsible for supporting the production of new biopharmaceuticals by performing analytical testing of samples from the production and stability programs and validating various analytical procedures according to ICH guidelines from clinical phase I/II to phase III and commercial. QC Chemistry performs analyzes for manufacturing and stability studies of the API and validation of analytical methods for clinical phase I/II and III.Within this broad working area and with various biopharmaceuticals, the QC area have a close collaboration with all departments across the organization.
Tasks and ResponsibilitiesAs equipment technician in QC Chemistry, you will be responsible for ensuring that our equipment is in service at all time. This you will do by planning and performing preventive cleaning, maintenance, and repair of our UHPLC equipment and equipment for CE-SDS and iCIEF. Furthermore, you should assist your colleagues in troubleshooting of analytical issues and be able to identify, analyze, diagnose issues and repair the equipment. You will also be responsible for the identification, purchase and qualification of new equipment and new equipment types in future expansions. The position requires hands-on experience with UHPLC maintenance and repair. All work in the department is performed under cGMP and you will be responsible for finalizing service reports and enter work performed in the equipment database. Your ProfileWe expect you to hold a degree as laboratory technician or similar and bring several years of work experience with equipment maintenance and repair and preferably with experience from the pharmaceutical industry.
In addition, we expect you to have:

  • Technical experience in (U)HPLC analysis, iCIEF and/or CE-SDS and experience with equipment maintenance
  • Experience with working in cGMP settings according to European and US regulatory guidelines
  • Experience in writing of Change Controls and SOP´s related to analytical equipment is an advantage
  • Good communication and interpersonal skills
  • Ability to interact positively within a team and in close collaboration with other working areas when needed

Applicants with practical experience in HPLC, iCIEF and/or CE-SDS analysis will be preferred. 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 OffersAGC 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! For further information about the position, please contact Team Lead Nina Lei, telephone +45 2269 9363, or Sr. Manager Eva Andersen, telephone +45 2760 2094. 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.


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