Global Manufacturing IT & Automation Lead (Hybrid)

Caraway Therapeutics, Inc.

Netherlands

Hybrid

EUR 90,000 - 130,000

Full time

8 days ago

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Benefits offered by this job

3% year-end allowance
Annual bonus
Solid pension plan
Company restaurant
Excellent accessibility (train and car

Job summary

Caraway Therapeutics, Inc. in Boxmeer (Netherlands) seeks a Manufacturing IT & Automation Project Lead to drive IT/automation initiatives across Boxmeer and De Bilt sites.

You will lead project planning, execution, and governance while developing project management competency within site teams. You will collaborate with Business Technology Partners to ensure timely delivery and alignment with GMP/validation requirements.

Qualifications

  • Bachelor’s degree in Engineering, Computer Science, or equivalent.
  • Minimum 2 years pharma experience.
  • Minimum 5 years experience with manufacturing IT/automation systems (PLCs/SCADA/historians/MES).
  • Minimum 5 years project management experience.

Responsibilities

  • Drive standardization of PM methodologies across IT/automation teams.
  • Lead project planning, scheduling, milestones, resources, and budgets.
  • Provide regular status updates to stakeholders.
  • Coordinate with IT, Operations, Engineering, Quality and vendors.
  • Provide technical guidance on PLC/SCADA/MES systems and automation.
  • Implement automation solutions and integration with existing systems.
  • Foster collaboration across IT divisions and global sites.

Skills

English fluency
Project management
Team collaboration
Communication

Education

Bachelor’s degree in Engineering/CS

Tools

MS Project

Job description

Caraway Therapeutics, Inc. in Boxmeer (Netherlands) seeks a Manufacturing IT & Automation Project Lead to drive IT/automation initiatives across Boxmeer and De Bilt sites.

You will lead project planning, execution, and governance while developing project management competency within site teams. You will collaborate with Business Technology Partners to ensure timely delivery and alignment with GMP/validation requirements.

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