Daytime Biopharma Manufacturing Associate

FLBD FUJIFILM Life Sciences Biotechnologies Denmark ApS; Hillerød; On-site; DKK 420,000 - 540,000; Full time

Benefits offered by this job

Fitness facilities

Canteen

Job summary

FUJIFILM Biotechnologies Denmark is seeking Daytime Operators (Manufacturing Associates) to join its biopharmaceutical production teams in Upstream and Downstream. The role offers a daytime schedule with no 3-shift rotation.

You will handle cGMP documents, batch documentation, in-process sampling, and equipment CiP/SiP, with training provided and opportunities to contribute to process improvements within GMP guidelines.

Qualifications

• Detail-oriented and thorough in following procedures.
• Proactive and takes initiative to address issues.
• Clear communication and keeping teammates informed.
• Reliable and trustworthy performer.
• Focused and diligent, even on routine tasks.
• Enthusiastic about working under GMP.
• Comfortable with equipment and processes in production.
• Able to read and understand work instructions in English.

Responsibilities

• Execute and revise cGMP documents.
• Complete batch documentation accurately.
• Perform in-process sampling and analytical measurements.
• Execute validation protocols.
• Assemble equipment.
• CiP/SiP of equipment.
• Train new colleagues.
• Report deviations and investigate root causes.
• Contribute to projects like process optimization, SOP updates, 5S, and continuous improvement.

Skills

Detail-oriented

Proactive

Clear communication

Reliable

GMP familiarity

Equipment handling

Reading English work instructions

Education

Life Science degree

Tools

cGMP documentation

SOPs

Chromatography

Filtration

Fermentation

Job description

FUJIFILM Biotechnologies Denmark is seeking Daytime Operators (Manufacturing Associates) to join its biopharmaceutical production teams in Upstream and Downstream. The role offers a daytime schedule with no 3-shift rotation.

You will handle cGMP documents, batch documentation, in-process sampling, and equipment CiP/SiP, with training provided and opportunities to contribute to process improvements within GMP guidelines.