Nightshift Bioprocess Operator: Upstream & Downstream

FLBD FUJIFILM Life Sciences Biotechnologies Denmark ApS; Hillerød; On-site; DKK 320,000 - 520,000; Full time

Job summary

FUJIFILM Biotechnologies is expanding its biopharmaceutical production teams in Hillerød, Denmark, inviting applicants for Nighttime Operator roles across Upstream, Downstream and Solution Preparation. You will participate in cGMP activities, handle batch documentation, perform sampling and contribute to validation and optimization projects.

The schedule includes night shifts with a training period, and prior experience in GMP or life sciences is a plus.

Qualifications

• You double-check the details and ensure nothing slips through the cracks.
• You take initiative and step in when something needs to be done.
• You explain things clearly, keep people in the loop, and learn new digital tools quickly.
• You can read and understand work instructions in English.
• Experience with GMP and SOPs is advantageous.
• Experience with cGMP, chromatography, filtration or fermentation is a plus.

Responsibilities

• Execute and revise cGMP documents.
• Handle and complete batch documentation.
• Perform in-process sampling and analytical measurements.
• Execute validation protocols.
• Mix solutions to support Upstream and Downstream operations.
• CiP/SiP of equipment.
• Train new colleagues.
• Report deviations.
• Contribute to process optimization or continuous improvements.

Skills

Attention to detail

Proactive approach

Clear communication

Read English work instructions

GMP/SOP awareness

Process understanding

Education

Life Science graduate

Job description

FUJIFILM Biotechnologies is expanding its biopharmaceutical production teams in Hillerød, Denmark, inviting applicants for Nighttime Operator roles across Upstream, Downstream and Solution Preparation. You will participate in cGMP activities, handle batch documentation, perform sampling and contribute to validation and optimization projects.

The schedule includes night shifts with a training period, and prior experience in GMP or life sciences is a plus.