Global QRA Lead: Quality, Regulatory & Compliance

Linde Middle East; Saudi Arabia; Sur place; SAR 90 000 - 130 000; Plein temps

Avantages offerts par ce poste

Restaurant d'entreprise

Indemnités de stage/alternance

Résumé du poste

Linde Sigas, a leader in medical gases, is seeking a QRA Manager in Saudi Arabia to oversee regulatory affairs and quality management across the Middle East. You will lead the QRA function, guide policy adoption in new markets, and ensure alignment with global governance standards.

You will drive continuous improvement of Quality Management Systems, collaborate with cross-functional teams, and negotiate regulatory requirements with authorities to protect patient safety and product integrity.

Qualifications

• Expertise in regulatory affairs, quality and pharmacovigilance.
• Experience with cross-cultural teams, external partners and authorities.
• Familiar with complex matrix structures, spanning regions and business segments.
• Fluent English required for the role.
• Lean/Six Sigma qualifications are an asset.
• Bachelor or Master in Pharmaceutical or equivalent.

Responsabilités

• Lead Quality and Regulatory Affairs activities in the Middle East, supporting new countries in policy adoption.
• Audit and monitor Quality Management Systems, driving continuous improvement and supplier compliance.
• Negotiate with regulatory bodies to influence medical gases and devices requirements.
• Develop and adapt quality management tools and coordinate working groups at regional and global levels.

Connaissances

Regulatory affairs

Quality

Pharmacovigilance

Cross-cultural teamwork

Matrix structures

English fluency

Lean Six Sigma

Pharma degree

QMS experience

Formation

Bachelor/Master in Pharmaceutical or equivalent

Description du poste

Linde Sigas, a leader in medical gases, is seeking a QRA Manager in Saudi Arabia to oversee regulatory affairs and quality management across the Middle East. You will lead the QRA function, guide policy adoption in new markets, and ensure alignment with global governance standards.

You will drive continuous improvement of Quality Management Systems, collaborate with cross-functional teams, and negotiate regulatory requirements with authorities to protect patient safety and product integrity.