Automation Data Systems Engineer - OT & PI Historian

Eli Lilly and Company

Katwijk

On-site

EUR 68,000 - 99,000

Full time

14 days+

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Benefits offered by this job

Company bonus
Healthcare benefits
Pension plan
Well-being benefits

Job summary

Eli Lilly and Company in Katwijk, Netherlands seeks an Automation Data Systems Engineer to support the Aveva PI Data Historian and related data systems. The role ensures reliability, compliance, and performance from project start through steady-state operations, with design integration into the global automation team before transitioning to a site-based process team.

Required: 5+ years in automation and in regulated pharma environments, 3+ years Aveva PI Data Historian administration, English

Qualifications

  • 5+ years in automation.
  • 5+ years in pharmaceutical or regulated industries.
  • Knowledge of GMPs and regulatory requirements.
  • 3+ years in Aveva PI Data Historian administration.
  • Experience with Windows OS, virtualization, and networking.

Responsibilities

  • Design, install, and qualify Aveva PI Data Historian and related data systems with internal teams.
  • Own system security, access controls, lifecycle management, and data integrity.
  • Perform audits and ensure compliance with quality and engineering standards.
  • Grow data platforms and support manufacturing process teams as new systems are added.
  • Collaborate with Corporate Automation, IT, and Information Security for lifecycle management.
  • Develop site procedures governing data systems.

Skills

Communication skills
Independent worker
Decision making
Problem solving
Organisational skills
Team collaboration

Education

Bachelor's degree in engineering or related science field

Tools

Aveva PI Data Historian
ISA S95
Citrix
VMware
Kepware
Matrikon
SQL Server
Microsoft OS
Virtual environments
Networking

Job description

Eli Lilly and Company in Katwijk, Netherlands seeks an Automation Data Systems Engineer to support the Aveva PI Data Historian and related data systems. The role ensures reliability, compliance, and performance from project start through steady-state operations, with design integration into the global automation team before transitioning to a site-based process team.

Required: 5+ years in automation and in regulated pharma environments, 3+ years Aveva PI Data Historian administration, English

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