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Laboratory Technician with Experience in HPLC and Capillary Electrophoresis (CE) Analysis of Proteins - 6-month temporary position

Laboratory Technician with Experience in HPLC and Capillary Electrophoresis (CE) Analysis of Proteins – 6-month temporary position

AGC is looking for Laboratory technicians with expertise with HPLC and CE analysis for protein based biotherapeutics.

We are seeking Laboratory technicians with experience in analysis of protein-based pharmaceuticals with capillary gel electrophoresis and HPLC techniques like size exclusion, ion exchange, hydrophobic interaction and/or affinity chromatography. The position is within our Analytical Development (AD) Department at AGC Biologics A/S (AGC). AGC is a Contract Manufacturing Organization with facilities in Denmark, Germany, Italy, Japan and USA and with customers all over the world.

 

The department

The AD Department is responsible for implementation, transfer and development of analytical procedures, analytical support to upstream and downstream, characterization of products, testing engineering batches for production and the transfer of analytical methods to QC for validation. AGC projects range from early pre-clinical development through all phases of clinical development all the way to commercial supply. AD is also involved in cross-functional project groups and implementation of new analytical technologies and techniques.

As a Laboratory technician in analytical development, you will be responsible executing a wide array of analytical methods with a focus on supporting our late stage and commercial projects, you will be responsible for generating the analytical results in the lab, processing the data and submitting it into our quality system for review by the department scientists. You will also be heavily involved in day-to-day tasks essential for the delivery of results, like preparation of buffers, preventive maintenance in instruments and all the work required to setting up large studies related to degradation and stability of the proteins of interest. You will be working together with an ever-growing team currently consisting of 5 scientists and 8 technician’s.

The work environment in our department is very informal. There is constant collaboration across the organization, and all employees have a professional and flexible attitude towards their work. The department consists of 30 dedicated and highly competent scientists and technicians working in four sub team; HPLC/CE development, bioassay development, process development support and characterization. The team is in close contact with our counterparts in our Seattle facility.

 

Responsibilities and tasks

As a Laboratory technician, you will be responsible for ensuring timely delivery of analytical results for a number of internal studies owned by AD as well as a number of supporting analytical work for our upstream and downstream development colleagues. You will also be heavily involved in setting up studies such as degradation studies and stability studies

You will get the opportunity to work with a broad range analytical techniques used in the analysis of protein based therapeutics.

 

The job includes:

  • Generation of analytical results by running HPLC and CE based methods in the lab
  • Data processing and reporting of data
  • Setting up supportive studies e.g. degradation and stability studies
  • Doing supportive tasks like manufacture of buffers, preventive maintenance on instruments etc.

 

Experience and competencies

The ideal candidate is a trained laboratory technician with industry experience in analyzing biopharmaceuticals. Alternatively, you holds at BSc, MSc or similar degree, in Protein Chemistry, Biochemistry, Biochemical or Chemical Engineering, and you are tired of sitting behind a desk all day, and want to get back into the laboratory. In addition to that, you have:

 

  • Experience in analysis of biologics, preferably from the biotech industry
  • Practical experience with running HPLC and capillary electrophoresis experiments
  • You are used to processing and reporting the data you generate in the lab
  • Experience with Chromeleon, or other part 11 compliant chromatography software is an advantage
  • Thorough understanding on HPLC troubleshooting and hands on experience with day-to-day preventive maintenance on HPLC systems is an advantage
  • You are self-driven, take initiative, and get things done
  • Excellent English written and oral communication skills are required as the company language is English.

 

On a personal level, we expect you to:

Be a high performing team player and to be ambitious on behalf of yourself and the company. You master the balance between speed of execution and quality of work. You embrace change and enjoy a rapid pace of work with a positive, can-do attitude and with a good sense of humor. You think of last minute changes as a positive variety in the daily work. You are driven by achieving results through others and are good at presenting results in a convincing manner.

 

AGC Biologics Copenhagen
AGC Biologics offers a dynamic working place and an excellent opportunity for working and growing with a varied array of tasks and challenges. You will get insight into and experience with the way the various departments throughout a biologics contract development and manufacturing organization interact in order to achieve success. Exciting and challenging assignments will keep coming your way, but you will to a large extent be able to plan your daily work on your own. AGC Biologics offers an informal working environment, where humor is part of the daily work life. We respect each other and our individual differences. AGC employees have a flexible attitude and we help each other to reach deadlines together as one team, in accordance with our slogan - Right. On Time.?

Application

We continuously evaluate incoming applications and conduct interviews accordingly. Therefore, please submit your application and CV as soon as possible. When the right candidates are found, the ad will close.

For further information, please contact Lasse Olsen, HPLC/CE Team lead, Analytical Development, phone +45 2269 9432, or Helle Grann Wendelboe, Senior Director of Analytical Development, phone +45 2294 3090.

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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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