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 pleasescrolldown
Er du en erfaren specialist inden for proteinanalyse der trives i et hurtigt og dynamisk biopharma-miljø Kan du levere robuste og højtkvalitative data selvstændigt i laboratoriet
Late-Stage Process Development tager ansvar for at føre processer sikkert fra sen klinisk fase til kommerciel produktion. Afdelingen består af tre specialiserede teams inden for upstream downstream og analytics med omkring 15 erfarne fagfolk i hvert team. Arbejdet er praktisk deadlines-orienteret og kræver tæt samarbejde på tværs af fagområder.
Rollen
SomPrincipalTechnician forventer vi at du allerede har solid erfaring med proteinanalyse i biopharma og kan tage ejerskab fra dag ét. Du vil arbejde med senfaseprogrammer hvor kvalitet robusthed og overholdelse af tidsplaner er altafgørende. Dit fokus vil være analytisk karakterisering og processtøtte primært med produkter fra pattedyrscellekulturer med enkelte mikrobiologiske opgaver.
Vi søger en person med flere års erfaring i et reguleret laboratoriemiljø som kan planlægge og gennemføre analytisk arbejde med minimal supervision.
Dine opgaver
Udføre og tage ansvar for analytiske assays der understøtter senfase procesudvikling med teknikker som SEC CIEX AIEX RP-HPLC HIC affinitetskromatografi CE-SDS og iCIEF.
Planlægge og prioritere eget arbejde i takt med projekt- og teambehov.
Selvstændigt behandle evaluere og klargøre analytiske data til videnskabelig gennemgang.
Dokumentere resultater i AGCs elektroniske systemer og bidrage til datafortolkning.
Vedligeholde fejlfinde og sikre pålidelig drift af analytiske instrumenter.
Arbejde tæt sammen med forskere og teknikere på tværs af analytics upstream og downstream.
Identificere og implementere forbedringer i arbejdsgange for øget fleksibilitet og effektivitet baseret på praktisk erfaring.
Vi forventer af dig
Uddannet laboratorietekniker eller tilsvarende teknisk baggrund. BSc eller MSc accepteres hvis karrieren tydeligt har været teknikerorienteret.
Minimum 5 års praktisk erfaring med proteinanalyse i biotech eller biopharma et ufravigeligt krav.
Stærk hands-on erfaring med HPLC-baserede metoder som SEC RP IEX HIC og affinitetskromatografi.
Solid erfaring med elektrophoretiske metoder som CE-SDS og iCIEF.
Indgående forståelse for analytisk instrumentering GMP-arbejde og dataanvendelse i senfaseudvikling og produktion.
Erfaring med Chromeleon er en fordel men ikke et krav.
Flydende engelsk både skriftligt og i dagligt samarbejde.
Pålidelig pragmatisk og selvkørende med en jordnær og professionel tilgang.
Ansøgning
Send dit CV hvis du mener du er den rette kandidat i en krævende og udviklende rolle. Vi opfordrer også til at søge hvis du ikke opfylder alle krav men føler at du kan bidrage. Har du spørgsmål så kontakt Fabio Michelet Manager Late-Stage Process Development på.
Bemærk at ansættelsesprocessen starter i uge 2 2026.
English version
Late-Stage Process Development
Are youan experienced protein analyticsprofessional ready to take ownership in a fast-paced late-stage biopharma environment Can you deliver robust high-quality data independently in the lab
Late-Stage Process Developmentis responsible fortaking processes from late clinical phase into commercial readiness. The department consists of three established teams across upstream downstream and analytics withroughly 15experienced professionals per team. The work is hands-on deadline-driven and highly collaborative across disciplines.
TheRole
This is aPrincipalTechnician role for someone who already knows protein analytics in a biopharma setting and canoperateindependently from day one. You will work withLate-Stage programs where dataquality robustness and timelines matter. The focus is analytical characterization and process support primarily for mammalian cellderived products with occasional microbial work.
This is not a training role.We are looking for someone who has spent several yearsin a lab environment understands regulated environments and can plan and execute analytical work with limited supervision.
WhatYoullDo
You will run and own analytical assays supporting late-stage process development using techniques including SEC CIEX AIEX RP-HPLC HIC affinity chromatography CE-SDS andiCIEF.
You will plan and prioritize your own work in alignment with project and team needs.
You will independently process evaluate and prepare analytical data for scientific review.
You will document results directly in AGCs electronic systems and contribute to data interpretation.
You willmaintaintroubleshootandensure reliable performance of analytical instruments.
You will work closely with scientists and technicians across analytics upstream and downstream.
You willidentifypractical improvements to workflows flexibility and efficiency based on hands-on experience.
What We ExpectfromYou
You are educated as a laboratory technician or have an equivalent technical background. A BSc or MSc is acceptable if your career path has been clearlytechnician focused.
You have at least 5 years of hands-on experience with protein analytics in biotech or biopharma. This is a firm requirement.
You havestrongpractical experience with HPLC-based protein methods such as SEC RP IEX HIC and affinity chromatography.
You have solid hands-on experience with electrophoretic methods such as CE-SDS andiCIEF.
You understand analytical instrumentation GMP-adjacent work and how data is used in late-stage development and manufacturing decisions.
Experience withChromeleonis a plus but not mandatory.
You communicate clearly in English both in writing and in daily collaboration.
You are reliable pragmatic and comfortable taking ownership. You contribute positively to the team and bring a grounded professional attitude.
Application
To apply pleasesubmityour CV. We encourage you to apply even if you do not meet every requirement.If you need further information about the position please feel free to contact Fabio MicheletManagerLate-StageProcess Developmenton
Please note that the hiring process for this role will begin in week2 2026.
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