(Danish version see below)

Laboratory Technician for QC Microbiology/Environmental monitoring in our Quality Control Department

Are you looking for new challenges in an international and inspiring environment?

The Department
The Quality Control unit at AGC Biologics A/S consist of; QC Bioassay, QC Chemistry, QC Microbiology, QC Raw Materials and QC Stability. QC Microbiology (consisting of 12 highly dedicated technicians and 6 scientists) is responsible for microbiological analysis on APIs for clinical and commercial samples, method validation, environmental monitoring in clean rooms, chemical/microbiological analyses on pharmaceutical water, and TOC analysis on rinse samples from production. The work is conducted under cGMP and AGC Biologics handle exciting customer projects from Phase I to Commercial stages.

The department works in close collaboration with Manufacturing, QA, Up- and Downstream Development, Analytical Development and external laboratories to maintain control of all steps in the manufacturing processes.  Everything we do, we do in close collaboration with our customers.

Tasks and Responsibilities
Your tasks will be environmental sampling incl. analyzing the samples further analyzing product in-process samples. Further also assist in administrative jobs e.g. review of data to EM reports.

Through testing and monitoring, you will help ensure maintenance of the required levels for environmental cleanliness in our clean rooms and that the manufactured products are of the expected microbiological quality and suitable for the intended purposes. You will have the opportunity to do investigations/support and follow-up on corrective/preventive actions in co-operation with Development and Manufacturing departments.

We are working on expanding our productions facilities and laboratories. It will therefore be possible to be involved in the qualification of clean rooms in our new facility. 

Your Profile
We expect you to hold a degree as laboratory technician or similar and preferably have some experience within the pharmaceutical industry. In addition, we expect you to bring some of the following experience and characteristics:
  • Experience with pharmaceutical microbiological analyses
  • Knowledge of environmental monitoring of clean rooms
  • Potential experience with LIMS
  • Experience with working cGMP
  • Have a high Quality mindset
  • Experience within review of data
  • A flexible, dynamic and excellent team player with good English and Danish skills
  • A good sense of humor and the ability to plan and complete your work independently and efficiently
  • Taking responsibility for your personal assignments and completing high quality work in a timely manner                                                                                          
AGC offers
AGC 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 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.
 

For further information regarding the position, please do not hesitate to contact Manager QC Microbiology Jakob Knudsen, telephone +45 27603029

We will process the applications as they arrive. Therefore, please submit your application and CV as soon as possible. You are welcome to submit either an English or Danish written applications and CV.

#JobsForUkraine 

 
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Quality control/miljømonitorering - Laborant/teknikker til QC Microbiologi

Leder du efter nye udfordringer i et international og inspirerende miljø? Vi skal udvide med en laborant/teknikker stilling

I AGC Biologics A/S (AGC), arbejder vi med udvikling af biopharmaceutiske produktions processer og GMP produktion af biopharmaceutiske proteiner til både kliniske test og kommercielt salg. Da vi er en kontrakt produktion organisation, er et højt niveau af service til vores kunder i fokus.

Afdelingen
Quality Control i AGC A/S består af : QC Bioassay, QC Chemistry, QC Microbiology, QC Raw Materials og QC Stability. QC Microbiology (med 12 dedikererede teknikkere/laboranter og 6 scientists) er ansvarlig for mikrobiologiske metode valideringer, analyse af produktions prøver både til kliniske forsøg og kommerciel produktion af drug substans. Derudover miljømonitorering (EM) af produktionsområder, kemiske/mikrobiologiske analyser af pharmaceutisk vand, og TOC analyser af rengøringsprøver fra produktionsudstyr.

QC Microbiologi er i tæt samarbejde med QC Bioassay, QC Chemistry, Analytical Development, Manufacturing, Up- & Downstream Development og Quality Assurance afdelingerne for at supportere alle trin i en produktionsproces.

Opgaver og Ansvar
Som Laborant/teknikker i QC Mikrobiologi vil du skulle tage miljømonitoreringsprøver (EM og vand) samt analyserer disse prøver, derudover også assistere i administrative opgaver f.eks. review af EM data.

Ved miljømonitorering og mikrobielle test af produktionsrum og produkter hjælper du med at sikre opretholdelse af krav til miljøet i vores rene rum, og de fremstillede produkter er af den forventede mikrobiologiske kvalitet.
Du vil få muligheder for, at foretage undersøgelser/support og lave opfølgninger til korrigerende/ forebyggende aktioner i forbindelse med mikrobielle miljø- og produkt-overskridelser, dette i samarbejde med udviklings- og produktionsafdelinger.

Da vi er i færd med at udvide vores produktionslinjer og laboratorier, vil det også være muligt at deltage i kvalificeringen af renrum i den nye facilitet.

Din Profil
Vi forventer du har en laborant uddannelse eller tilsvarende og har noget erhvervserfaring inden for Mikrobiologi/miljømonitorering gerne fra en kvalitetsafdeling/pharmaceutisk industri. Derudover forventes der:
  • Erfaring med farmaceutiske mikrobiologiske analyser
  • Erfaring med miljømonitering i klassificerede områder
  • erfaring med LIMS
  • Høj kvalitetssans og erfaring med review af data
  • En god sans for humor og evnen til at planlægge og afslutte dit arbejde selvstændigt og effektivt til tiden i den rette kvalitet
  • Erfaring med at arbejde under cGMP
  • Evne for at interagere positivt i et team og i tæt samarbejde med andre Laboranter og Scientists
  • Evne for at kommunikere professionelt både skriftligt og mundtligt på dansk og engelsk
AGC tilbyder
AGC tilbyder en dynamisk arbejdsplads med gode muligheder for, at arbejde med mange forskellige opgaver og udfordringer. Du vil få indsigt i og erfaring med den måde forskellige afdelinger i en kontraktproduktionsorganisation arbejder sammen for at opnå succes.

Spændende og udfordrende opgaver vil konstant tilgå Quality Control, og du vil i høj grad selv kunne planlægge dit daglige arbejde. AGC tilbyder et uformelt arbejdsmiljø, hvor humor er en del af det daglige arbejdsliv. Vi respekterer hinanden og hinandens forskelligheder. AGC’s ansatte har en fleksibel attitude og vi hjælper hinanden for at nå deadlines sammen som et team

Send din ansøgning så snart som muligt og ikke senere end 30. aug. 2022. Vi behandler ansøgningerne som vi modtager dem, og kvalificerede ansøger kan forvente at blive indkaldt til samtale før deadline.  

For mere information angående stillingen, kontakt Manager for QC Microbiology, Jakob Knudsen, telephone +45 27603029. Du er velkommen til at sende ansøgning og CV på dansk eller engelsk.

 

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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