Planning, coordinating, and executing global Regulatory Affairs and Product Environmental Compliance programs
Ensuring that GLO Operations are compliant with applicable regulatory requirements related to environmental product compliance
Leading global RA & PEC programs applicable to Global Logistics
Establishing and maintaining program governance, including scope definition, milestones, risk management
Coordinating implementation of Product Environmental Compliance (PEC) requirements impacting logistics
Acting as the official correspondent to relevant health authorities for GLO sites
Evaluating impact of changing global regulations
Supporting compliance with applicable regulations such as Packaging and Packaging Waste Regulation

Hon. Bachelor’s degree in Science, Engineering or related subject or equivalency is mandatory
Masters degree in Science, Engineering or related subject is preferred
Regulatory Affairs Certification (RAC) in medical devices is preferred
8+ years of experience in Regulatory Affairs, Product Environmental Compliance, or regulatory program management within a regulated industry (medical devices preferred)
Demonstrated experience managing complex, cross‑functional, global programs
Working knowledge of EU environmental, packaging, and battery regulations and their impact on logistics and distribution activities
Experience working within ISO 13485 / MDR / FDA‑regulated quality systems
Experience supporting distribution, logistics, or supply chain activities is preferred

Program Manager, Product Environmental Compliance – Regulatory Affairs

Key skills