Laboratory technicians with experience in Bioassays for Process Development (PD) support
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AGC is looking for two technicians with expertise and experience in analysis of protein based biotherapeutics.
We are seeking a technician with a background and interest in analytical chemistry and more specifically bioassay methodology such as ELISA, Octet, qPCR, SDS-PAGE, pH, OD and LAL for a varied and exciting position in the Process Development Support (PD) Team in the Analytical Development (AD) Department at AGC Biologics A/S (AGC) as we are expanding the team. 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 consists of 43 dedicated and highly competent scientists and technicians working in four sub teams; chromatographic assay development, bioassay development, Process Development (PD) support, and characterization. AD is responsible for implementation, transfer and development of analytical procedures, analytical support to upstream and downstream process development, 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. The AD department is in close contact with our counterparts in our Seattle, Boulder, Heidelberg and Chiba facilities.
As a technician in the PD Support team, you will be working with Bioassay, like ELISA, Octet, qPCR, SDS-PAGE, pH, OD and LAL. All in the quest to support a wide variety of protein based products to support our customers getting their product to market as fast as possible with a high quality. You will be working together with a team of 2 scientists and 12 technician’s. As a technician in AD you will be running a high number of samples in support of the process development areas. We can promise an exciting and diverse job.
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.
Responsibilities and tasks
You will get the opportunity to work with a broad range of personalities as well as diverse products in different clinical stages, you will also get the opportunity to use your skills in a cross-functional setting and interactive environment.
The job includes:
- Running analytical assays to generate data to support process development.
- Independent processing of analytical data and preparing it for scientist review.
- Trouble-shooting.
- Department responsibilities
- Instrument responsibilities
Experience and competencies
The ideal candidate is an educated lab technician or has an equivalent scientific/technical background. You have practical experience with running methods within bioassay in a protein context. In addition to this you have:
- 2-5 years of experience in analytics for biologics, preferably from the biotech industry.
- Understanding of analytical instrumentation.
- An understanding of biopharmaceutical manufacturing and regulatory requirements.
- Good interpersonal and communication skills.
- Excellent English communication skills.
- Computer skills
- Experience in software such as Gen5 or SoftMax Pro will be an advantage
On a personal level we expect you to:
Be a team player and to be ambitious on behalf of yourself, the team, and the company. You are result driven and embrace change and enjoy a rapid pace of work with a positive, can-do attitude and with a good sense of humor.
For further information, please contact Keith McCall, PD Support Team Leader, Analytical Development, phone +45 2760 3041, or Helle Grann Wendelboe, Senior Director of Analytical Development, phone +45 2294 3090.
We will process the applications as they arrive. Therefore, please submit your application and CV as soon as possible.
AGC Biologics offers a highly competitive compensation package and a friendly, collaborative culture that values personal initiative and professional achievement.
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.
Information og data
Denne ledige stilling har jobtypen "Laborant", og befinder sig i kategorien "Sundhed og forskning".
Arbejdsstedet er beliggende i København
Jobbet er oprettet på vores service den 3.2.2022, men kan have været deaktiveret og genaktiveret igen.
- Laborant
- København
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