(Senior/Principal) Technician, Late Stage Process Development at AGC Biologics

Copenhagen, Capital Region of Denmark, Denmark -

Full Time

Start Date

Immediate

Expiry Date

22 Mar, 26

Salary

0.0

Posted On

22 Dec, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Protein Purification, Downstream Techniques, Chromatography, Ultrafiltration, Centrifugation, cGMP, Analytical Methods, Communication, Teamwork, Problem-Solving, Process Optimization, Flexibility, Proactivity

Industry

Pharmaceutical Manufacturing

Description

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 spille en central rolle i at bringe avancerede biologiske lægemidler fra udvikling til markedet? Vi søger en erfaren Downstream Technician (Senior/Principal) til vores Late-Stage (Fase III) Process Development team. Det er ikke en entry-level stilling. Din ekspertise får direkte betydning for procesopskalering og kommerciel beredskab. I Late-Stage Process Development teamet arbejder vi med at skalere processer fra klinisk til kommerciel produktion. Vi udfører robusthedsstudier, kvalifikation af scale-down modeller, proceskarakterisering og studier af resinens livscyklus. Du bliver en del af et team bestående af dygtige teknikere og forskere, som samarbejder tæt med Analytical Method Development og Manufacturing for at sikre høj kvalitet og skalerbare processer. Rollen Vi søger en laboratorieekspert med solid erfaring inden for downstream-proces. Dine opgaver vil blandt andet være: Udførelse af praktiske eksperimenter inden for klaring, centrifugering, kromatografi og ultrafiltrering Vedligeholdelse og kalibrering af laboratorieudstyr Samarbejde med tværfunktionelle teams for at støtte proceskarakterisering og opskalering Bidrage til teknisk problemløsning og procesoptimering Hvad vi forventer af dig Minimum 3 års erfaring med proteinrensning i udviklings- eller pilotlaboratorier Dokumenteret erfaring med downstream-teknikker som kromatografi, ultrafiltrering og centrifugering Erfaring med cGMP er en klar fordel Kendskab til analytiske metoder som UV/VIS, HPLC, CE og SDS Stærke kommunikations- og samarbejdsevner samt flydende engelsk, både skriftligt og mundtligt Fleksibel, proaktiv og vant til at arbejde i et dynamisk og hurtigt miljø Ansøgning Send dit CV, hvis du mener du er den rette kandidat. Erfaring og kompetence tæller mere end at opfylde alle krav. Har du spørgsmål? Kontakt Silvia Pirrung på spirrung@agcbio.com eller Fabio Michelet på fmichelet@agcbio.com. Ansættelsesprocessen starter i uge 2, 2026. [English Version] Do you want to play a key role in bringing advanced biologics from development to market? We’re looking for a hands-on, experienced Downstream Technician (Senior/Principal) to join our Late-Stage (Phase III) Process Development team. This is not an entry-level role; your expertise will directly impact process scale-up and commercial readiness. Our Late-Stage Process Development team brings processes from clinical to commercial manufacturing. We run robustness studies, scale-down model qualification, process characterization, and resin lifetime studies. You’ll join a team of skilled technicians and scientists working closely with Analytical Method Development, Process Transfer & Validation and Manufacturing to ensure high-quality, robust processes. The Role We need a lab professional with solid experience in downstream processing. You will: Execute hands-on experiments in clarification, centrifugation, chromatography, and ultrafiltration Maintain and calibrate lab equipment Collaborate with cross-functional teams to support process characterization Contribute to technical problem-solving and process optimization What We Expect from You 3+ years of protein purification experience in development or pilot-scale labs Proven practical skills with downstream techniques (chromatography, ultrafiltration, centrifugation) cGMP experience is highly valued Familiarity with analytical methods (UV/VIS, HPLC, CE, SDS) Strong communication and teamwork skills; fluent in English (spoken and written) Flexible, proactive, and able to thrive in a dynamic, fast-paced environment Application To apply, submit your CV. We value depth of experience over meeting every box perfectly. Questions? Contact Silvia Pirrung at spirrung@agcbio.com or Fabio Michelet at fmichelet@agcbio.com. The hiring process for this role begins week 2, 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 2,500 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 www.agcbio.com. 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. AGC Biologics is a global CDMO headquartered in Seattle, Washington, USA. The company provides pharmaceutical development and manufacturing services for protein-based biologics, cell and gene therapies, messenger RNA. With locations across three continents, we specialize in the following modalities and substances: mammalian and microbial-based therapeutic proteins, plasmid DNA (pDNA), messenger RNA (mRNA), viral vectors, and genetically engineered cells. Our services range from process development, analytical development, cGMP manufacturing, quality control and quality assurance, and process validation.

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Responsibilities

The role involves executing hands-on experiments in downstream processing, maintaining and calibrating lab equipment, and collaborating with cross-functional teams. The technician will also contribute to technical problem-solving and process optimization.