Not specified; pyy ranges determined by role, leve...
Onsite
8+ years regulatory affairs experience
Gmp requirements knowledge
Health authority audit leadership
Agilent is seeking a Regulatory Site Lead for their Glostrup manufacturing site. This senior role focuses on providing regulatory leadership in a manufacturing context, ensuring compliance and efficiency in operations
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, inspection readiness, and managing site changes effectively.
Candidates must possess a strong understanding of GMP requirements and demonstrate the ability to translate complex regulatory guidance into practical actions.
Matching Summary
Match Score: 85
Agilent is seeking a Regulatory Site Lead for their Glostrup manufacturing site. This senior role focuses on providing regulatory leadership in a manufacturing context, ensuring compliance and efficiency in operations.
Salary
Not specified; Pay ranges determined by role, level, and location; Individual pay determined by work location and additional factors
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 science or engineering
IVD or medical device background
Matrixed organization experience
Solutions-oriented mindset
Strong analytical communication skills
Key Requirements
Bachelor's degree in scientific or engineering discipline
8+ years of regulatory affairs experience
Experience with IVDs or medical devices
Proven track record supporting regulatory inspections