Sr. Associate I, Regulatory Affairs Strategy

At Alcon, we are driven by the meaningful work we do to help people see brilliantly. We innovate boldly, champion progress, and act with speed as the global leader in eye care. Here, you’ll be recognized for your commitment and contributions and see your career like never before. Together, we go above and beyond to make an impact in the lives of our patients and customers. We foster an inclusive culture and are looking for diverse, talented people to join Alcon.

As a Senior Associate Regulatory Affairs supporting the EMEA Regulatory Operations team, you will be trusted to work on regulatory compliance, dossier development, and product registration activities across a diverse portfolio in Riyadh.

Please note that for this position Saudi nationals are preferred.

In this role, a typical day will include:

• Collaborating with regional affiliates and cross-functional teams to address regulatory requirements and health authority inquiries across the Middle East and EMEA region
• Preparing and managing regulatory dossiers, submissions, licensing activities, and labeling documentation for pharmaceuticals, medical devices, cosmetics, and food supplements
• Maintaining accurate and up-to-date submission databases, ensuring timely approvals and compliance tracking
• Supporting clinical trial disclosure and submission publishing activities with high attention to quality and regulatory standards
• Ensuring full adherence to GxP requirements, SOPs, and documentation standards to maintain audit readiness and regulatory compliance
  
  

WHAT YOU’LL BRING TO ALCON:

• Bachelor’s or Master’s degree in Biomedical Engineering, Life Sciences, or a related field
• Minimum 3 years of experience in Regulatory Affairs within the Middle East region in a multinational medical or pharmaceutical company
• Strong knowledge of regulatory frameworks in the Middle East; understanding of EU regulations is highly desirable
• Proven ability to manage regulatory submissions, dossier preparation, and compliance documentation
• Excellent collaboration, communication, and influencing skills within matrix organizations
• Fluency in English and Arabic (written and spoken)
• High level of organization, adaptability, and a proactive, solution-oriented mindset
  
  

HOW YOU CAN THRIVE AT ALCON:

• Work in a dynamic, international environment with exposure to diverse product categories and regulatory landscapes
• Take ownership of meaningful projects that directly impact patient safety and product accessibility across markets
• Collaborate with a highly skilled, supportive team where innovation, continuous improvement, and personal growth are encouraged
  
  

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