QRA Manager

Responsibilities

• Lead Quality and Regulatory Affairs (QRA) for the Middle East region, ensuring compliance with medical management systems and company policies.
• Develop, adapt, and implement quality system management tools and Standard Operating Procedures (SOPs) to meet local and regional needs.
• Manage and motivate the ME QRA team, fostering professional development and excellence in performance.
• Execute, monitor, and audit Quality Management Systems (QMS) for RBU Healthcare, including internal and supplier audits.
• Support regulatory strategies for EMEA & REE Healthcare products to drive business growth and compliance.
• Represent QRA in regional management teams and participate in global quality governance working groups.
• Act as a decision-maker regarding potential non-compliance issues to prevent liability risks and ensure patient safety.
• Support new countries in adopting quality policies for the marketing and production of medicinal gases and regulated products.

Requirements

• University bachelor’s or master’s degree in Pharmaceutical sciences or an equivalent field.
• 3+ years of experience in the pharmaceutical or medical devices industry.
• Proven expertise in regulatory affairs, quality management, and pharmacovigilance.
• Hands-on experience with the implementation and maintenance of Quality Management Systems (QMS).
• Fluency in English.
• Experience working with cross-cultural teams, external partners, and regulatory authorities.
• Ability to navigate complex matrix organizational structures.

Preferred Qualifications

• Lean or Six Sigma qualification.
• Experience with Medical Device Regulation (MDR).

About the Company

Linde is a global leader committed to technologies and products that unite customer value with sustainable development. We prioritize safety, responsibility toward society, and an inclusive environment where experts can thrive through continuous learning and development.