Bioanalytikere/Laboranter til Afdeling for Klinisk Mikrobiologi, afsnittet for serologi- og molekylærbiologi, Herlev Hospital

• Har interesse for immunhistokemi/histologi, gerne med erfaring inden for disse områder
• Er selvstændig og har gode samarbejdsevner
• Er fleksibel og ansvarsbevidst med fokus på faglig kvalitet til gavn for patienterne
• Har flair for teknisk udstyr
• Har sans for orden og systematik
• Har lyst til positivt at præge din arbejdsplads

• Et job med fokus på optimal behandling af den enkelte patient
• Et godt fagligt og socialt miljø med gode og aktive kollegaer
• Et job med udviklingsmuligheder inden for de forskellige laboratoriefaglige områder i afdelingen
• En god introduktionsperiode med grundig oplæring

Jnr. 148591

Would you like to be part of a team within the manufacturing area at AGC in Søborg. You might be the one we are looking for!

AGC Biologics

AGC Biologics is an international and modern organization with production sites in Europe, Japan, and the US. AGC Biologics is the largest contract development and manufacturing organization (CDMO) in the world, and currently AGC Biologics employs more than 900 people worldwide whereof 430 are situated in Denmark at the site in Søborg. AGC Biologics delivers biopharmaceutical development and manufacturing of Drug Bulk Intermediates/Active Pharmaceutical Ingredients for clinical studies as well as for the market.

The position

You will become part of the manufacturing area consisting of five production lines, which produce pre-clinical, clinical, and commercial products for a wide variety of customers from around the world. You will be part of a group of highly dedicated technicians and scientists working with various stakeholders such as QA, QC and Development.

As a Technician within the upstream team, you will plan and perform cell culture steps in the manufacturing process.

You will be working with these tasks among others:

• Preparation of media and feeds.
• Performance of seed train.
• Set up and use of single-use bioreactors 500L / 2000L and daily sampling.
• Harvest using Cuno filters and Millistack filters.
• Perfusion using ATF.

Your responsibility will include preparation of production rooms and production systems before use, clean up and line change over after use, as well as participation in qualification, maintenance, and calibration of upstream process equipment.

Together with the team, you are responsible for the delivery of cell cultures to further processing in the downstream team, and for ensuring batch documentation of high quality in close collaboration with QA/QC.

Experience and competencies

The candidate we are looking for has the following qualifications:

• A trained Technician, preferably a process technologist, with hands-on experience from cell cultivation, if you have experience with mammalian cell cultivation this will be an advantage.
• Has experience from working in a GMP regulated production and following written procedures.
• Has experience with process optimization.
• Has an interest in the maintenance of equipment.
• Has excellent collaboration competencies.
• The ability to speak and write English.

As a person, you have a positive mindset, and are flexible and enjoy taking on new tasks and responsibilities. You thrive in a dynamic environment and can cope with uncertainties.

Practical information

It is a full-time position based in Søborg, Denmark
Normally, work hours are on dayshift (7-16) and cover regular weekend shifts, but it can vary so you must be able to work outside normal work hours.

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.  

• er ansvarlig for den daglige drift
• sikrer en høj faglige kvalitet i afsnittets funktioner
• er ansvarlig for kvalitetssikring af GMP-renrum og vedligeholdelse af udstyr
• indgår i produktionen af celler til immunterapi (herunder tumor-infiltrerende lymfocytter og CAR T celler) i renrum
• indgår i produktionen af kræftvacciner i renrum.

• et arbejde, hvor du gør en vigtig forskel for behandlingen af patienter med cancer.
• et kreativt og ambitiøst team med forståelse for, at de bedste resultater skabes i et godt arbejdsmiljø
• dygtige og interesserede kolleger
• indflydelse og ansvar indenfor dit arbejdsområde
• at lære dig nye teknikker
• at imødekomme din lyst til personlig udvikling, herunder muligheden for faglig udvikling inklusiv kursus-deltagelse.
• en spændende arbejdsplads, hvor medarbejdere og ledere har fokus på kvalitet
• en arbejdsplads, der er i konstant udvikling, og hvor vi hurtigt tilpasser os nye krav og forventninger

• er uddannet bioanalytiker med flere års erfaring
• er ambitiøs og har lyst til og let ved at lære nye ting
• er grundig og har sans for detaljen
• har gode samarbejdsevner, er fleksibel og ansvarsbevidst
• gerne har ansvarsmæssig erfaring
• gerne har erfaring med cellebiologiske teknikker
• gerne har erfaring med GMP
• gerne har erfaring med renrums-arbejde
• er fleksibel i forhold til eventuelle skæve arbejdstider i forbindelse med patientbehandling.

Jnr. 148846

Join a dynamic and international company in Søborg where everyone is responsible for delivering right on time as one team!

AGC Biologics A/S (AGC) develops biopharmaceutical processes and run GMP production of pharmaceutical proteins from early state test until commercial production. As AGC is a Contract Manufacturing Organization (CMO), the customer is in centrum and AGC has a high level of service to their customers.

As AGCs new technician in Manufacturing, you will be part of a professional and dedicated team consisting of both Scientists and technicians. You will experience a very dynamic working environment with a high variety of tasks and an environment where cGMP production never becomes routine. The department work in close collaboration with other teams and departments who are dependent on the solutions and services we deliver.

Responsibilities and tasks

As a member of AGCs “Solution Preparation & Production Support team” you will work with:
- Preparation and filtration of buffer solutions and upstream media from small scale (< 5 kg) to large scale (up to 2000 kg).
- Daily Planning of work, ordering of raw materials and disposables, approval of finalized buffers and medias
- Simple analytical methods as pH, conductivity, Osmolality etc.
- Transport and surface sanitization of production equipment and disposables.
- Daily control and responsibility for equipment and rooms

We are continuously working on improvements and optimization of existing processes and routines, and support a strong learning environment where we within a relatively short time become familiar with a variety of new processes and technologies.

Experience and competencies

You have a technical and/or a laboratory background, are a proactive team player, flexible and positive, and you:

- Can work according to written procedures in English
- Have experience with cGMP/GDP and working according to quality documents.
- Can work independently and with responsibility for own tasks.
- Have experience with work in clean rooms.
- Can work in an organization with constant customer audits and inspections.

As AGCs corporate language is English, all procedures and GMP related documents are in English. It is therefore important that you can read English without problems, and we also appreciate the ability to speak English at a certain level.

AGC offers

AGC offers a dynamic working place with good opportunities of working with a varied array of tasks and challenges in Manufacturing. 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.

Practical information

It’s a full-time position.
- The work will be on day/evening/weekend shift according to shift plan.
- We offer a 3- 12 month contract.
- The position is based in Søborg, Denmark

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.