GMP Manufacturing Equipment Coordinator

AGC Biologics, Inc.; København; Hybrid; DKK 350,000 - 520,000; Full time

Job summary

AGC Biologics, Inc. in Søborg, Copenhagen area, seeks a Senior Technician, Manufacturing (Day Shift) to coordinate preventive maintenance and act as a liaison between Production and Engineering. The role focuses on keeping equipment across Buffer, Upstream, and Downstream in compliant, high‑quality operation.

You will work within a cross‑functional team, supporting documentation, and rapid escalation when issues occur, ensuring production stays on schedule and quality standards are met.

Qualifications

• Technical background in a relevant field such as process, mechanical, or industrial tech.
• Experience coordinating maintenance tasks or serving as liaison between departments.
• Experience in GMP-regulated or biotech/pharma manufacturing recommended.
• Strong English written and spoken communication.

Responsibilities

• Maintain overview of equipment status, maintenance plans, and tasks for Buffer, Upstream, and Downstream.
• Coordinate preventive maintenance with Engineering and production.
• Act as a key contact between production units and Engineering for planned maintenance and breakdowns.
• Escalate issues quickly to minimize downtime and support repair efforts.
• Contribute to documentation, logbooks, and maintenance records per GMP.
• Participate in deviation handling and investigations related to equipment.
• Support continuous improvement of maintenance processes and cross-functional collaboration.
• Plan and execute transport of equipment.

Skills

Technical background

Maintenance coordination

Cross-functional collaboration

English communication

Problem solving

Tools

CMMS systems

Job description

AGC Biologics, Inc. in Søborg, Copenhagen area, seeks a Senior Technician, Manufacturing (Day Shift) to coordinate preventive maintenance and act as a liaison between Production and Engineering. The role focuses on keeping equipment across Buffer, Upstream, and Downstream in compliant, high‑quality operation.

You will work within a cross‑functional team, supporting documentation, and rapid escalation when issues occur, ensuring production stays on schedule and quality standards are met.