Summary
At Linde, the Quality and Regulatory Affairs Manager will lead quality and regulatory activities across the Middle East and support the adoption of policies in new countries. The role includes auditing Quality Management Systems, driving continuous improvement and supplier compliance, and addressing non-compliance issues to protect patient safety. The manager will build and develop the QRA team, coordinate regional and global working groups, and contribute to quality governance and strategy. Business travel for customer visits, audits and compliance support is part of the role.
The posting
As published on linde.com. Pulled from the employer's site and shown as they wrote it.
In this role, you will act in line with Linde's Integrity criteria and ensure compliance with medical Management System policies You will conduct business trips for customer visits, audits, and compliance support Manage administrative duties and training completion for Quality and Regulatory Affairs employees And you will shape and implement quality strategies within REE and EMEA through leadership participation Provide input to global Quality governance and promote Quality initiatives across regions You will develop and adapt quality management tools and coordinate working groups at regional and global levels Lead Quality and Regulatory Affairs activities in the Middle East, supporting new countries in policy adoption Build and lead a competent QRA team, fostering professional development and regulatory compliance Audit and monitor Quality Management Systems, driving continuous improvement and supplier compliance Negotiate with regulatory bodies to influence medical gases and devices requirements and decide on non-compliance issues to protect patient safety