Alcon

Sr. Associate, Regulatory Affairs Operations, Middle East

Alcon  •  Riyadh, SA (Onsite)  •  3 hours ago
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Job Description

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 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

Alcon Careers
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About Alcon

Alcon helps people see brilliantly. As the global leader in eye care with a heritage spanning over 75 years, we offer the broadest portfolio of products to enhance sight and improve people’s lives. Our Surgical and Vision Care products touch the lives of more than 260 million people in over 140 countries each year living with conditions like cataracts, glaucoma, retinal diseases and refractive errors. Our more than 25,000 associates are enhancing the quality of life through innovative products, partnerships with Eye Care Professionals and programs that advance access to quality eye care. Learn more at www.alcon.com.

Industry
Manufacturing & Production
Company Size
10,000+ employees
Headquarters
Geneva, CH
Year Founded
Unknown
Website
alcon.com
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