Technician for QC Chemistry, HPLC/Chromatographic analysis

Do you thrive in a dynamic environment, in a department with skilled colleagues in an organization where we work as one team? If yes – you might be our new technician in QC Chemistry and be part of a growing global CDMO! 
QC Chemistry at AGC Biologics A/S is expanding and looking for a technician for HPLC/Chromatographic analysis to support manufacturing and stability studies.

The job
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.
QC Chemistry is one of five departments in the QC area, where we are responsible for supporting the production of new biopharmaceuticals by performing analytical testing of samples from the production and stability programs and validating various analytical procedures according to ICH guidelines from clinical phase I/II to phase III and commercial. 
Within this broad working area and with various biopharmaceuticals, the QC area have a close collaboration with all departments across the organization.

Tasks and responsibilities
As technician in QC Chemistry, you will be responsible for performing HPLC analysis such as RP-UHPLC, SE-UHPLC, HIC-UHPLC, cIEX-UHPLC, CE-SDS, peptide mapping and iCIEF. 
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 cGMP settings according to European and US regulatory guidelines 
  • Good communication and interpersonal skills 
  •  Ability to interact positively within a team and in close collaboration with other working areas when needed

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. We will process the candidates as they arrive. Therefore, please submit your application and CV as soon as possible. When the right candidates are found, the add will close. We are therefore looking forward to receive your application today! ______________________________________________________________________________________________ Leder du efter nye udfordringer i en afdeling med dygtige og inspirerende kolleger og et højt niveau af samarbejde i en kontraktproducerende virksomhed i høj vækst? 
QC Chemistry i AGC Biologics A/S udvider og søger en laborant med erfaring inden for HPLC/kromatografi til analyse af prøver bl.a. fra produktionen og til stabilitetsstudier.

  

Afdelingen
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.
QC Chemistry er en ud af fem afdelinger i QC og er ansvarlig for analytiske metodevalideringer i henhold til ICH guidelines, analyse af produktionsprøver og stabilitetsprøver samt frigivelse af drug substans. Vi arbejder tæt sammen med de andre QC-afdelinger samt Analytical Development, Manufacturing, Up- & Downstream Development og Quality Assurance 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. Vi udfører både planlagte analyser fra produktionen og stabilitetsstudier af API, samt valideringer af analytiske metoder til klinisk 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 er laborantuddannet og har flere års erhvervserfaring indenfor Quality Control eller analytical development. Derudover forventes det, at du har:

  • Erfaring med udførelse af UHPLC, iCIEF og/eller CE-SDS analyser
  • Erfaring med at arbejde under cGMP
  • Gode kommunikations- og samarbejdsevner  
  • Egenskaberne til at interagere positivt i et team og i tæt samarbejde med andre laboranter og scientists 
  • Egenskaberne 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. Derudover 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.Vi holder samtaler løbende og indtil den rette kandidat er fundet, send derfor din ansøgning hurtigst muligt. 

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.
About AGC Biologics
AGC Biologics is a global Contract Manufacturing Organization (CMO) with biomanufacturing facilities in Europe, Japan 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. AGC Biologics also offers non-exclusive license to CHEF1™, a proprietary CHO cell line development platform. CHEF1 delivers stable, high-titer, production-quality cell lines in optimized time frames. It is the foundation of CMC Biologics’ innovative approach to cell line and process development.
Visit www.agcbio.com to learn why AGC Biologics is a World Leader in process development and contract manufacturing.


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