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Our purpose is to bring hope to life by enabling life-changing therapies for patients around the globe creating a healthier and happier tomorrow. Our mission is to work side by side with our customers in order to improve patients lives by bringing new biopharmaceuticals to market.
For English version please scroll down
Vil du hjlpe kunder med at bringe avancerede biologiske produkter p markedet Trives du i en rolle hvor du kan lre og udvikle dig Vrdstter du teamwork og elsker at vre en del af et tvrfagligt team Hvis ja er denne rolle som (Principal/Senior) Downstream Tekniker i vores afdeling for Late stage (fase III) procesudvikling den perfekte mulighed for dig.
Om afdelingen
Afdelingen for Late stage-procesudvikling spiller en central rolle i overgangen fra klinisk skala til kommerciel produktion. Vi bestr af tre teams af teknikere og forskere som arbejder med robusthedsstudier kvalificering af nedskaleringsmodeller proceskarakterisering resin-lifetime studier og lignende.
Du bliver en del af et engageret team og vil f ansvar for eksperimenter og laboratoriearbejde i vores downstream-laboratorium. Vi arbejder med bde mammale og mikrobielle cellelinjer og samarbejder tt med interne afdelinger som Analytical Method Development og Manufacturing.
Om rollen
Vi sger en laborant med praktisk erfaring i downstream-teknikker. Du kommer til at arbejde med:
Klarificering / Centrifugering
Kromatografi
Ultrafiltrering
Kvalifikationer
5 rs erfaring med proteinoprensning
Kendskab til udviklings- eller pilotskala laboratorier
Fordel med erfaring i cGMP-milj
Interesse for analytiske metoder (UV/VIS HPLC CE SDS)
Teknisk forstelse og vedligehold af laboratorieudstyr
Gode samarbejds- og kommunikationsevner
Engelsk p skrift og tale
Positiv fleksibel og klar til nye opgaver
Trives i et dynamisk milj
Ansgning
Upload dit CV du er velkommen til at sge selvom du ikke opfylder alle krav.
Vi vurderer ansgninger lbende.
Ved sprgsml kontakt Tove Christensen p eller Ligia Gomes at
English Version
Do you want to help customers bring advanced biological products to market
Do you thrive in a role where you can learn and grow Do you value teamwork and love being part of a cross-functional team If so this position as a (Principal/Senior) Downstream Technician in our Late-stage (Phase III) Process Development department is the perfect opportunity for you.
About the Department
The Late-Stage Process Development Department plays a key role in scaling processes from clinical to commercial manufacturing. We consist of three teams of technicians and scientists working with robustness studies scale-down model qualification process characterization and resin lifetime studies.
You will join a highly dedicated team and be responsible for executing experiments and hands-on lab work in our downstream lab. We work with both mammalian and microbial cell lines and collaborate closely with departments such as Analytical Method Development and Manufacturing.
The Role
Were looking for a trained lab technician with practical experience in downstream techniques. Youll be working with:
Clarification / Centrifugation
Chromatography
Ultrafiltration
Qualifications
5 years of experience with protein purification
Background in development or pilot-scale labs
Experience with cGMP is a plus
Interest in analytical methods (UV/VIS HPLC CE SDS)
Comfortable with maintenance/calibration of lab equipment
Excellent teamwork and communication skills
Fluent in English (spoken and written)
Positive flexible and ready to take on new tasks
Able to adapt in a dynamic environment
Application
Submit your CV we encourage applications even if all requirements arent met.
Applications are reviewed on an ongoing basis.
Our culture at AGC Biologics is defined by the six core values: Knowledge Trust Quality Ingenuity Accountability and Teamwork. Our core values stem from our team members and are embedded into our DNA. They provide a common language and understanding of how we as an organization are connected across three continents. Our core values serve as a compass and reminder of how we achieve our purpose of bringing hope to life for patients around the globe.
AGC Biologics is a leading global biopharmaceutical Contract Development and Manufacturing Organization (CDMO) with a strong commitment to delivering the highest standard of service as we work side-by-side with our clients and partners every step of the way. We provide world-class development and manufacture of mammalian and microbial-based therapeutic proteins plasmid DNA (pDNA) messenger RNA (mRNA) viral vectors and genetically engineered cells. Our global network spans the U.S. Europe and Asia with cGMP-compliant facilities in Seattle Washington; Boulder and Longmont Colorado; Copenhagen Denmark; Heidelberg Germany; Milan Italy; and Chiba Japan. We currently employ more than 2500 employees worldwide. Our commitment to continuous innovation fosters the technical creativity to solve our clients most complex challenges including specialization in fast-track projects and rare diseases. AGC Biologics is the partner of choice. To learn more visit.Want to keep posted about our growth and learn more about our company Follow us on LinkedIn and give us a quick Like on Facebook!
AGC Biologics offers a highly competitive compensation package and a friendly collaborative culture that values personal initiative and professional achievement. AGC Biologics is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age ancestry color family or medical care leave gender identity or expression genetic information marital status medical condition national origin physical or mental disability political affiliation protected veteran status race religion sexual orientation or any other characteristic protected by applicable laws regulations and ordinances.
Required Experience:
Staff IC
Full-Time