Biopharma Maintenance Technician – Shift Roles

AstraZeneca

Dublin

On-site

EUR 42,000 - 56,000

Full time

6 days ago
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Job summary

AstraZeneca's Dublin Bulk Drug Substance Facility is seeking a skilled Maintenance Technician to join a high-performing biopharmaceutical manufacturing team. In this hands-on role you will maintain, troubleshoot and optimise critical process equipment, supporting continuous improvement and start-up activities.

You'll work within a GMP environment, using CMMS and Lean tools to reduce downtime and improve equipment reliability, with shift rotation including weekends.

Qualifications

  • Significant maintenance experience on process equipment in cGMP environments.
  • Strong troubleshooting and problem-solving abilities.
  • Familiar with GMP/regulatory requirements for maintenance.
  • Experience using CMMS and MS Office tools.

Responsibilities

  • Perform scheduled and reactive maintenance on process equipment per site procedures.
  • Troubleshoot technical issues to minimise downtime and improve performance.
  • Ensure compliance with EHS, quality and cGMP standards.
  • Utilise CMMS and other tools to manage maintenance activities.
  • Support CAPAs, investigations and process safety initiatives.
  • Assist in creating/updating maintenance procedures, plans and training materials.
  • Support equipment installation, qualification, start-up and validation.
  • Act as SME across multiple process technologies and share best practices.
  • Analyse data to identify improvement opportunities and reliability gains.
  • Lead or support Lean-driven continuous improvement projects (5S, Root Cause Analysis).
  • Coordinate maintenance work by external vendors and contractors.

Skills

Maintenance experience
Troubleshooting
CMMS experience
Communication skills

Education

Technical certification in Mechanical/Electrical or related discipline

Tools

CMMS
Microsoft Office

Job description

AstraZeneca's Dublin Bulk Drug Substance Facility is seeking a skilled Maintenance Technician to join a high-performing biopharmaceutical manufacturing team. In this hands-on role you will maintain, troubleshoot and optimise critical process equipment, supporting continuous improvement and start-up activities.

You'll work within a GMP environment, using CMMS and Lean tools to reduce downtime and improve equipment reliability, with shift rotation including weekends.

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