Associate Director, Digital Manufacturing Systems & Operations It

539

Boxmeer, Netherlands
Competitive salary; 3% year-end allowance; annual ...
Hybrid
Gmp compliance and 21 cfr part 11 knowledge
Leadership of agile product teams
Experience with sap s/4hana and mes systems
The Associate Director, Digital Manufacturing Systems & Operations IT role at a biotechnology company in Boxmeer, Netherlands, focuses on leading a team responsible for ensuring compliance and reliability in manufacturing systems. The position emphasizes digital transformation, operational excellence, and collaboration across departments in a highly regulated environment

Job Summary

  • This role leads a team responsible for delivering reliable, compliant operational support for manufacturing systems in a highly regulated GMP environment.
  • The successful candidate will define and execute a 3–5-year digital transformation roadmap aligned with business objectives and global strategy.
  • Candidates must act as the primary IT subject-matter expert during audits and inspections while managing critical systems like LIMS, SAP, and MES.

Matching Summary

Match Score: 85

The Associate Director, Digital Manufacturing Systems & Operations IT role at a biotechnology company in Boxmeer, Netherlands, focuses on leading a team responsible for ensuring compliance and reliability in manufacturing systems. The position emphasizes digital transformation, operational excellence, and collaboration across departments in a highly regulated environment.

Salary

Competitive salary; 3% year-end allowance; Annual bonus based on performance

Skills & Requirements

Must-have

  • GMP Compliance and 21 CFR Part 11 knowledge
  • Leadership of agile product teams
  • Experience with SAP S/4HANA and MES systems
  • Regulatory audit and inspection support
  • Application lifecycle management expertise
  • Data integrity and validation processes

Nice-to-have

  • Experience with Machine Learning and AI
  • Knowledge of IIoT and Robotics
  • SAFe or advanced Agile certification
  • Strategic planning in regulated environments
  • Vendor and third-party integration skills

Key Requirements

  • Master's degree plus 6 years experience OR Bachelor's plus 8 years
  • Minimum 5 years of people management experience
  • Proven experience in biologics or pharmaceutical industries
  • Prior experience leading regulatory inspections or audits
  • Certification or experience in ITIL, Agile, or SCRUM

Work Rights

Not specified

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