Senior Technician, Late Stage Process Development

at  AGC Biologics

København, Region Hovedstaden, Denmark -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate19 Feb, 2025Not Specified19 Nov, 2024N/ACommunication Skills,Laboratory Techniques,English,Chromatography,Ultrafiltration,Laboratory Equipment,Sds PageNoNo
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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.
Do you want to help customers bring advanced biological products to market? Do you thrive in a role where you can learn and develop? If so, this role as Principal Technician in our Late-Stage Process Development team could be the perfect opportunity for you.
About the Department & Team
Our Late-Stage Process Development Department plays a pivotal role in transitioning processes from clinical-scale to commercial manufacturing. The department is comprised of three dedicated teams. As part of a group of highly skilled technicians and scientists, you will collaborate on process characterization and optimization projects. You’ll experience a close-knit team environment that fosters collaboration across various technical disciplines.
We develop processes for products derived from both mammalian and microbial cell lines, working closely with key stakeholders such as Analytical Method Development and Manufacturing. You’ll be joining a dynamic and flexible workplace with numerous opportunities to contribute and grow professionally.
About the Role

We’re seeking a trained laboratory technician (Laborant) with hands-on experience in fundamental laboratory techniques. Your primary tasks will include conducting experiments and practical downstream lab work using the following technologies:

  • Clarification/Centrifugation
  • Chromatography
  • Ultrafiltration

Your Qualifications

  • Solid experience in protein purification methods.
  • Background in development laboratories or pilot-scale production.
  • Familiarity with working in a cGMP environment.
  • Experience with analytical methods such as UV/VIS Spectrophotometry, UHPLC, and SDS-PAGE.
  • Interest in maintaining and calibrating laboratory equipment.
  • Excellent collaboration and communication skills.
  • Fluency in English, both written and verbal.
  • A positive mindset with flexibility and enthusiasm for taking on new tasks and responsibilities.
  • Ability to thrive in a dynamic environment and adapt to uncertainties.

Application

  • To apply, please submit your CV. We encourage you to apply, even if you do not meet every requirement.
  • If we see a potential match, one of our recruiters will contact you to discuss your application.
  • If both sides remain positive after this discussion, we will move forward to the assessment stage to evaluate the key skills required for the job.
  • For more information, please contact Hiring Manager, Tove M.I.E. Christensen at +45 2294 3019.

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

Responsibilities:

  • Clarification/Centrifugation
  • Chromatography
  • Ultrafiltratio


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Information Technology/IT

Pharma / Biotech / Healthcare / Medical / R&D

Technician

Graduate

Proficient

1

København, Denmark