Senior Equipment Engineer: Lifecycle & Validation

Get 360Pharma

Leiden

On-site

EUR 55,000 - 85,000

Full time

14 days+

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Job summary

Get 360Pharma in Leiden, Netherlands is seeking an Equipment Engineer to act as system owner for assigned equipment and drive lifecycle, asset management, and maintenance governance. You will lead installation, qualification, validation, and ongoing operation of equipment and systems, ensuring GMP compliance and robust documentation.

You will collaborate with Operations, Engineering, Quality, and other stakeholders to support production needs while driving improvements in safety, quality,

Qualifications

  • Bachelor-level HBO degree with at least 3 years of relevant experience in a regulated environment.
  • Experience as system owner or equipment engineer with lifecycle management responsibilities.
  • Experience introducing new equipment or systems, including validation and user requirements.
  • Familiarity with GMP, data integrity, audits, and documentation practices.

Responsibilities

  • Act as system owner and SME for assigned equipment and systems, supporting lifecycle management and maintenance governance.
  • Lead installation, qualification, validation, and ongoing operation of new equipment and systems.
  • Maintain asset data, identify risks, and align maintenance plans with production schedules.
  • Investigate equipment failures via root cause analysis and drive cross-functional improvements.
  • Ensure GMP compliance and maintain documentation, SOPs, and audit readiness.
  • Support training, Gemba walks, and safety, quality, reliability, and scheduling improvements.

Skills

Equipment lifecycle management
Asset management
Maintenance governance
GMP compliance
Root cause analysis
Stakeholder management
Data analysis
MS Office

Education

HBO degree (or equivalent)

Tools

Documentation systems

Job description

Get 360Pharma in Leiden, Netherlands is seeking an Equipment Engineer to act as system owner for assigned equipment and drive lifecycle, asset management, and maintenance governance. You will lead installation, qualification, validation, and ongoing operation of equipment and systems, ensuring GMP compliance and robust documentation.

You will collaborate with Operations, Engineering, Quality, and other stakeholders to support production needs while driving improvements in safety, quality,

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