Senior Mammalian Downstream Technician — Night Shift

AGC Biologics, Inc.; København; Hybrid; DKK 420,000 - 540,000; Full time

Benefits offered by this job

Pension

Health insurance

Canteen

Employee Club

Discounts

Job summary

AGC Biologics in Copenhagen is seeking a Senior Technician for Mammalian Downstream Manufacturing on the night shift. You will execute downstream purification steps, operate chromatography systems including UNICORN, and ensure GMP-compliant documentation while collaborating with a cross-functional team.

Ideal candidates have 3–5 years in GMP manufacturing, with hands-on chromatography, filtration and UF/DF experience, and a commitment to quality and continuous improvement in a GMP environment.

Qualifications

• 3–5 years of GMP-regulated manufacturing experience in biotech/pharma.
• Experience with chromatography, filtration, and UF/DF processes in a GMP setting.
• Strong documentation practices and aseptic technique.

Responsibilities

• Execute downstream purification processes including chromatography, filtration and UF/DF.
• Operate chromatography systems, including UNICORN, applying technical understanding during production.
• Ensure accurate GMP documentation and compliance with procedures and aseptic practices.
• Support troubleshooting, deviation investigations and continuous improvement activities.
• Own training, technical qualifications, and development; share knowledge with colleagues.

Skills

Downstream purification

GMP experience

Independent worker

Team collaboration

Education

Process Operator

Industrial Technician

Biotechnology Technician

Tools

UNICORN software

Job description

AGC Biologics in Copenhagen is seeking a Senior Technician for Mammalian Downstream Manufacturing on the night shift. You will execute downstream purification steps, operate chromatography systems including UNICORN, and ensure GMP-compliant documentation while collaborating with a cross-functional team.

Ideal candidates have 3–5 years in GMP manufacturing, with hands-on chromatography, filtration and UF/DF experience, and a commitment to quality and continuous improvement in a GMP environment.