Regulatory Site Lead, Glostrup

Agilent Technologies Inc

Glostrup, Denmark
Not specified; pyy ranges determined by role, leve...
Onsite
8+ years regulatory affairs experience
Gmp requirements knowledge
Health authority audit leadership
Agilent Technologies Inc. is seeking a Regulatory Site Lead for its Glostrup manufacturing site, focusing on regulatory leadership in manufacturing, compliance, and inspection readiness. The ideal candidate should have extensive regulatory affairs experience within regulated environments and strong communication skills

Job Summary

  • This role provides on-site regulatory leadership for the Glostrup manufacturing site, ensuring regulatory considerations are embedded early into operations.
  • The Regulatory Site Lead serves as the primary interface for health authority audits, customer inspections, and site changes while maintaining inspection readiness.
  • Candidates must possess strong analytical skills to translate complex regulatory requirements into practical guidance for cross-functional teams including Manufacturing and Quality.

Matching Summary

Match Score: 85

Agilent Technologies Inc. is seeking a Regulatory Site Lead for its Glostrup manufacturing site, focusing on regulatory leadership in manufacturing, compliance, and inspection readiness. The ideal candidate should have extensive regulatory affairs experience within regulated environments and strong communication skills.

Salary

Not specified; Pay ranges determined by role, level, and location; Individual pay based on skills and experience

Skills & Requirements

Must-have

  • 8+ years regulatory affairs experience
  • GMP requirements knowledge
  • Health authority audit leadership
  • Post-approval change management
  • Manufacturing site regulatory interface

Nice-to-have

  • Advanced degree in scientific discipline
  • IVD or medical device background
  • Matrixed organization experience
  • Solutions-oriented mindset
  • Strong analytical communication skills

Key Requirements

  • Bachelor's degree in science or engineering
  • 8+ years in regulated manufacturing environments
  • Experience with IVDs or medical devices
  • Demonstrated audit and inspection support experience

Work Rights

Not specified

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