Are you looking for an exciting job in an international company producing new biological medicines? Do you want to work in a dynamic environment together with skilled colleagues and in an organization where everyone is responsible for delivering right-on-time as one team?

Quality Control, Bioassay is looking for a Technician to join our team responsible for Reference Materials.

About the department
Bioassay is part of the Quality Control (QC) organization which consists of 120 dedicated colleagues in six departments: Bioassay, Chemistry, Microbiology, Adjuvant, Stability and Raw Materials . We are responsible for method validations for early and late stage products, release analysis of clinical batches as well as commercial as well as analysis of raw materials and stability programs. We are working in an international and customer oriented way to secure fast and reliable manufacturing of medicines to our customers.
 
Role and Responsibilities
As Technician you will work closely together with the Principal Scientist responsible for our reference material within QC. You can look forward to a great deal of responsibility and varied work tasks. You will be part of a really good team in an open and informal environment with solid professionalism, high pace and lots of good laughs.

You will be involved in a wide range of exciting tasks and challenges;

  • Responsible for inventory control of reference material
  • Responsible for equipment maintenance
  • Involved in preparation and release testing of reference material
  • Support in the daily housekeeping of the laboratories
  • Take ownership of ad hoc tasks ensuring on-time completion
  • Collaboration with colleagues within QC organization
  • All tasks must be performed in cGMP compliance
Qualifications
The ideal candidate holds a degree as technician (laborant). We expect you to have a structured mindset, be able to work independently and used to meet tight deadlines with a can-do attitude but without compromising the quality.

In addition, we expect you to bring some of the following experience and characteristics:

  • Experience working in a GMP environment
  • Good communication skills and a service-minded attitude as you will work closely together with your colleagues in QC
  • Has a flair for teamwork combined with the ability and desire to work independently
  • Thrive in a fast-paced environment, able to handle mulitple tasks simultaneously

Application
For further information regarding the position, please contact Director Henriette S. Nielsen, QC Bioassay, at +45 2294 3092. We treat the applications as we receive then, and conduct interviews with qualified candidates. When the right candidates are found, the add will close.

AGC offers
AGC offers a dynamic working place with good opportunities of working with a varied array of manufacturing 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 extent 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.

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

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