Quality Control Laborant til QC Chemistry

Quality Control Laborant til QC Chemistry

(Please see English version below)

Leder du efter nye udfordringer i et internationalt og inspirerende område?
QC Chemistry udvider med 1 Laborant i en 12 måneders midlertidig stilling

I AGC Biologics A/S (AGC) arbejder vi med udvikling af biofarmaceutiske produktionsprocesser og GMP-produktion af biofarmaceutiske proteiner til både kliniske tests og kommercielt salg. Da vi er en kontraktproducerende virksomhed, har vi fokus på at levere et højt niveau af service til vores kunder.

Afdelingen
QC-afdelingen i AGC består af tre grupper: QC Bioassay, QC Chemistry og QC Microbiology.
QC Chemistry er ansvarlig for analytiske metodevalideringer, analyse af produktionsprøver, frigivelse af drug substans, analyse af stabilitetsprøver, koordinering af stabilitetsstudier, prøveudtagelse og test af råvarer. Vi arbejder tæt sammen med QC Bioassay, QC Microbiology, Analytical Development, Manufacturing, Up- & Downstream Development og Quality Assurance afdelingerne for at supportere alle trin i en produktionsproces.

Opgaver og Ansvar
Som Laborant i QC Chemistry vil du primært arbejde med HPLC-analyser, såsom RP-UHPLC, SE-UHPLC, HIC-UHPLC, cIEX-UHPLC, Peptide mapping, samt CE-SDS og iCIEF analyser. Vi udfører både planlagte analyser fra produktionen og stabilitetsstudier af API, samt valideringer af analytiske metoder til kliniske fase I/II og III. Alt arbejde udføres under cGMP. Du vil få ansvar for HPLC-udstyr i QC og hjælpe med at sikre, at eksisterende procedurer bliver fulgt.

Din Profil
Vi forventer, at du har en laborantuddannelse og har flere års erhvervserfaring indenfor Quality Control eller analytical development. Derudover forventes der:
• Erfaring med udførelse af UHPLC, iCIEF og/eller CE-SDS analyser
• Erfaring med at arbejde under cGMP er en fordel
• Gode kommunikations- og samarbejdsevner.
• Evne til at interagere positivt i et team og i tæt samarbejde med andre Laboranter og Scientists
• Evne til at kommunikere professionelt både skriftligt og mundtligt på dansk og engelsk

Ansøgere med praktisk erfaring med HPLC, iCIEF og/eller CE-SDS analyser vil blive foretrukket.
Det er vigtigt at have en selv-motiverende personlighed med en pragmatisk attitude og tilgang til det daglige arbejde –uden at gå på kompromis med kvaliteten. Ydermere, trives du i et udfordrende og dynamisk miljø og nyder et højt arbejdstempo. Du har en positiv og proaktiv attitude og en god fornemmelse for humor.

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 kontraktproducerende organisation arbejder sammen for at opnå succes.
Quality control modtager konstant spændende og udfordrende opgaver, 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 d. 21. december 2019. Vi behandler ansøgninger løbende, og kvalificerede ansøgere kan forvente at blive indkaldt til samtale før deadline.

For mere information angående stillingen, kontakt Teamlead Nina Lei, telefon +45 2269 9363 eller Director, QC Chemistry, Iben Schildt Sørensen, telefon +45 2294 2949.

Technician for QC Chemistry, working with Chromatographic analysis

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

QC Chemistry is expanding and looking for a Technician for a temporary 12 month position, covering HPLC/Chromatographic analysis to support manufacturing and stability studies.

At AGC Biologics A/S (AGC), we work with the development of biopharmaceutical manufacturing processes and GMP manufacturing of biopharmaceutical proteins for both clinical testing and marketing. Since we are a contract manufacturing organization, a high level of service to our clients is in focus.

The Department
The QC department at AGC Biologics consists of three functional groups: QC Bioassay, QC Chemistry, and QC Microbiology. The QC groups are responsible for supporting the production of new biopharmaceuticals by controlling raw materials, performing analytical methods, planning and executing stability programs and validating various analytical procedures according to ICH guidelines from clinical phase I to phase III and commercial.
Within this broad working area and with various biopharmaceuticals, QC have a close collaboration with departments across the organization to gain control of all steps in the manufacturing processes.

Tasks and Responsibilities
As a Technician in QC Chemistry, HPLC & Chromatographic you will be responsible for performing HPLC analysis, such as RP-UHPLC, SE-UHPLC, HI-UHPLC, cIEX-UHPLC, and CE-SDS, Peptide mapping and iCIEF analysis.

The position requires experience within HPLC/ Chromatographic analysis.
QC Chemistry performs analyzes for manufacturing and stability studies of the API, and validation of analytical methods for clinical phase I/II and III. All work is performed under cGMP. You will be responsible for equipment in QC and should help to ensure that existing procedures and guidelines are followed.

Your Profile
We expect you to hold a degree as laboratory technician or similar and bring several years of work experience within analytical development or quality control as a laboratory technician. In addition, we expect you to have:
• Technical experience in (U)HPLC analysis, iCIEF and/or CE-SDS
• Experience with working in GMP environment is an asset
• Good communication and interpersonal skills.
• Ability to interact positively within a team and in close collaboration with other working areas when needed
• Good communication and interpersonal skills.
Applicants with practical experience in HPLC, iCIEF and/or CE-SDS analysis will be preferred.
It is important to have a self-motivating personality with a pragmatic attitude and approach to the daily work - without compromising quality. Furthermore, you thrive in a challenging and dynamic environment and enjoy a rapid pace of work. You bring a positive, can-do attitude and a good sense of humor.

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 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.

Send your application as soon as possible and not later than 21th December 2019. We treat the applications as we receive them, and qualified applicants can expect to be interviewed before the deadline.

For further information regarding the position, please do not hesitate to contact Team lead Nina Lei, telephone +45 2269 9363, or Director, QC Chemistry, Iben Schildt Sørensen, telephone +45 2294 2949.