Laborant til QC General Chemistry
4 months ago
Er du en dygtig laborant og kunne du tænke dig at arbejde for en hurtig voksende CDMO? Vi leder efter en laborant, der deler vores passion, drive og energi – det vi kalder Genki – Er det dig vi søger til vores team?
QC General Chemistry teamet består i øjeblikket af 20 dedikerede medarbejdere (12 laboranter, 4 kemikere, 1 manager, 1 Associate Manager, 1 laborant praktikant og 2 studentermedhjælpere). Teamet analyserer In proces, Drug substance (DS) og Drug product (DP) til frigivelse af lægemidler globalt for vores kunder. Vi arbejder med mange forskellige kemiske analyser fra de simple til mere komplicerede f.eks. UV, GelChip, SoloVPE, OSMO, pH, SDS-page, icIEF, CE-SDS, AAS. Derudover supporterer vi produktionen med vand og swab analyser til frigivelse af produktionsudstyr (konduktivitet, pH og TOC). Med de mange nye kunder er en anden vigtig del af vores opgaver at sikre metodeoverførsler og kvalificering af nye kundespecifikke metoder og forbedringer af eksisterende metoder i samarbejde med vores Analytical Development afdeling. Derudover udfører vi kvalificering af kontroller og referencestandarder, håndterer afvigelser, CAPA'er, invalid assays, og meget mere. Alt dette er en del af vores daglige arbejde med at sikre kvaliteten af vores kunders lægemidler og sikre leverance til patienterne.
Om stillingen
Dine primære opgaver vil blandt andet være:
- Analytisk test af In-proces, DS, DP og stabilitetsprøver i laboratoriet i henhold til cGMP
- Deltage ved overførsel af nye metoder til vores QC-laboratorium i samarbejde med teamets kemiker
- Fejlfinding i laboratoriet hvis den analytiske test fejler
- Dokumentation og gennemgang af testresultater i vores LIMS system
- Generel laboratoriearbejde i et cGMP-laboratorium inkl. SOP-opdateringer, kvalificering af reagenser til analytisk testning, vedligeholdelse af analytiske instrumenter, indkøb og modtagelse af laboratorievare (kemikalier, kits etc.)
- Bidrage til et sikkert og sundt arbejdsmiljø
Kvalifikationer og uddannelse
• Du har en uddannelse som laborant
• Den ideelle kandidat har nogle års erfaring med QC kemiske analyser i et ISO/GxP reguleret laboratorium men det er ikke et krav.
Vi søger en person med can-do-attitude og energi og som forstår kravene i et cGMP QC-laboratorium. En der kan håndtere en travl hverdag med skiftende prioriteringer uden at miste det gode humør og overblik. Som person besidder du fremragende samarbejdsevner og forstår behovet for at arbejde tæt sammen i teamet – vi hjælper hinanden for at lykkes med vores fælles mål. Du er nysgerrig, selvkørende, dedikeret og systematisk og kan planlægge din dag i laboratoriet på en struktureret måde. Du sætter pris på at arbejde i et team, hvor der er plads til faglig diskussion samt et godt grin. Gode engelskkundskaber er en forudsætning, da engelsk er vores virksomhedssprog.
Er det lige dig vi står og mangler, så kan vi tilbyde dig et spændende og udfordrende job i en virksomhed der går en spændende fremtid i møde med mange nye kunder og produkter og store muligheder for personlig udvikling og ansvar. Har du samtidig lyst til at indgå i et fantastisk team af kompetente og engagerede medarbejdere er du den rigtige kandidat.
Om FUJIFILM Diosynth Biotechnologies og vores kvalitetskontrol (QC) afdeling
FUJIFILM Diosynth Biotechnologies er verdens ledende kontraktproducent af biologisk medicin (CDMO). Vi servicerer kunder i medicinalindustrien – fra prækliniske undersøgelser til kommerciel GMP-produktion. Vores overordnet mission er “Advancing Tomorrow’s Medicines” og vi vil gerne invitere dig til at være en del af denne rejse.
Ansøgning
Har dette vakt din interesse? Så upload venligst dit CV og ansøgning hurtigst muligt da vi evaluerer ansøgninger løbende. For yderligere information kontakt Associate Manager Sidsel Schrøder på mail eller på telefon 41 94 99 20.
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